SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF

[0001] Any and all applications for which a foreign or domestic priority claim is identified, for example, in the Application Data Sheet or Request as filed with the present application, are hereby incorporated by reference under 37 CFR 1.57, and Rules 4.18 and 20.6.

[0002] 1. Field

[0003] The present application relates to the fields of chemistry, biochemistry and medicine. More particularly, disclosed herein are nucleotide analogs, pharmaceutical compositions that include one or more nucleotide analogs and methods of synthesizing the same. Also disclosed herein are methods of treating diseases and/or conditions with a nucleotide analog, alone or in combination therapy with one or more other agents.

[0004] 2. Description

[0005] Nucleoside analogs are a class of compounds that have been shown to exert antiviral and anticancer activity both in vitro and in vivo, and thus, have been the subject of widespread research for the treatment of viral infections. Nucleoside analogs are usually therapeutically inactive compounds that are converted by host or viral enzymes to their respective active anti-metabolites, which, in turn, may inhibit polymerases involved in viral or cell proliferation. The activation occurs by a variety of mechanisms, such as the addition of one or more phosphate groups and, or in combination with, other metabolic processes.

[0006] Some embodiments disclosed herein relate to a compound of Formula (I) or a pharmaceutically acceptable salt thereof.

[0007] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a hepatitis C viral (HCV) infection that can include administering to a subject identified as suffering from the HCV infection an effective amount of one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for ameliorating and/or treating a HCV infection. Still other embodiments described herein relate to one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, that can be used for ameliorating and/or treating a HCV infection.

[0008] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, in the manufacture of a medicament for ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof, that can be used for ameliorating and/or treating a HCV infection by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s).

[0009] Some embodiments disclosed herein relate to a method of inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, in the manufacture of a medicament for inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof, that can be used for inhibiting replication of a hepatitis C virus by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s).

[0010] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include administering to a subject identified as suffering from the HCV infection an effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, another antiviral compound, a compound of Formula (AA), a compound of Formula (BB), a compound of Formula (CC) and a compound of Formula (DD), or a pharmaceutically acceptable salt of any of the foregoing. Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include contacting a cell infected with the HCV infection with an effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, another antiviral compound, a compound of Formula (AA), a compound of Formula (BB), a compound of Formula (CC) and a compound of Formula (DD), or a pharmaceutically acceptable salt of any of the foregoing. Some embodiments disclosed herein relate to a method of inhibiting replication of a hepatitis C virus that can include administering to a subject identified as suffering from a HCV infection an effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, another antiviral compound, a compound of Formula (AA), a compound of Formula (BB), a compound of Formula (CC) and a compound of Formula (DD), or a pharmaceutically acceptable salt of any of the foregoing. In some embodiments, the agent can be a compound, or a pharmaceutically acceptable salt thereof, selected from Compound 1001-1016, 2001-2012, 3001-3014, 4001-4012, 5001-5011, 6001-6078, 7000-7027, 8000-8016 and 9000-9105, or a pharmaceutical composition that includes one or more of the aforementioned compounds, or a pharmaceutically acceptable salt of the foregoing. In some embodiments, the method can include administering a second agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, another antiviral compound, a compound of Formula (AA), a compound of Formula (BB), a compound of Formula (CC) and a compound of Formula (DD), or a pharmaceutically acceptable salt of any of the foregoing.

[0020] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. All patents, applications, published applications and other publications referenced herein are incorporated by reference in their entirety unless stated otherwise. In the event that there are a plurality of definitions for a term herein, those in this section prevail unless stated otherwise.

[0021] As used herein, any “R” group(s) such as, without limitation, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ represent substituents that can be attached to the indicated atom. An R group may be substituted or unsubstituted. If two “R” groups are described as being “taken together” the R groups and the atoms they are attached to can form a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heterocycle. For example, without limitation, if R^a and R^b of an NR^a R^b group are indicated to be “taken together,” it means that they are covalently bonded to one another to form a ring:

In addition, if two “R” groups are described as being “taken together” with the atom(s) to which they are attached to form a ring as an alternative, the R groups are not limited to the variables or substituents defined previously.

[0022] Whenever a group is described as being “optionally substituted” that group may be unsubstituted or substituted with one or more of the indicated substituents. Likewise, when a group is described as being “unsubstituted or substituted” if substituted, the substituent(s) may be selected from one or more the indicated substituents. If no substituents are indicated, it is meant that the indicated “optionally substituted” or “substituted” group may be substituted with one or more group(s) individually and independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), heteroaryl(alkyl), (heterocyclyl)alkyl, hydroxy, alkoxy, acyl, cyano, halogen, thiocarbonyl, O-carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, S-sulfonamido, N-sulfonamido, C-carboxy, O-carboxy, isocyanato, thiocyanato, isothiocyanato, nitro, silyl, sulfenyl, sulfinyl, sulfonyl, haloalkyl, haloalkoxy, trihalomethanesulfonyl, trihalomethanesulfonamido, an amino, a mono-substituted amino group and a di-substituted amino group.

[0023] As used herein, “C_a to C_b” in which “a” and “b” are integers refer to the number of carbon atoms in an alkyl, alkenyl or alkynyl group, or the number of carbon atoms in the ring of a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heterocyclyl group. That is, the alkyl, alkenyl, alkynyl, ring of the cycloalkyl, ring of the cycloalkenyl, ring of the aryl, ring of the heteroaryl or ring of the heterocyclyl can contain from “a” to “b”, inclusive, carbon atoms. Thus, for example, a “C₁ to C₄ alkyl” group refers to all alkyl groups having from 1 to 4 carbons, that is, CH₃—, CH₃CH₂—, CH₃CH₂CH₂—, (CH₃)₂CH—, CH₃CH₂CH₂CH₂—, CH₃CH₂CH(CH₃)— and (CH₃)₃C—. If no “a” and “b” are designated with regard to an alkyl, alkenyl, alkynyl, cycloalkyl cycloalkenyl, aryl, heteroaryl or heterocyclyl group, the broadest range described in these definitions is to be assumed.

[0024] As used herein, “alkyl” refers to a straight or branched hydrocarbon chain that comprises a fully saturated (no double or triple bonds) hydrocarbon group. The alkyl group may have 1 to 20 carbon atoms (whenever it appears herein, a numerical range such as “1 to 20” refers to each integer in the given range; e.g., “1 to 20 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 20 carbon atoms, although the present definition also covers the occurrence of the term “alkyl” where no numerical range is designated). The alkyl group may also be a medium size alkyl having 1 to 10 carbon atoms. The alkyl group could also be a lower alkyl having 1 to 6 carbon atoms. The alkyl group of the compounds may be designated as “C₁-C₄ alkyl” or similar designations. By way of example only, “C₁-C₄ alkyl” indicates that there are one to four carbon atoms in the alkyl chain, i.e., the alkyl chain is selected from methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl and t-butyl. Typical alkyl groups include, but are in no way limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, pentyl and hexyl. The alkyl group may be substituted or unsubstituted.

[0025] As used herein, “alkenyl” refers to an alkyl group that contains in the straight or branched hydrocarbon chain one or more double bonds. An alkenyl group may be unsubstituted or substituted.

[0026] As used herein, “alkynyl” refers to an alkyl group that contains in the straight or branched hydrocarbon chain one or more triple bonds. An alkynyl group may be unsubstituted or substituted.

[0027] As used herein, “cycloalkyl” refers to a completely saturated (no double or triple bonds) mono- or multi-cyclic hydrocarbon ring system. When composed of two or more rings, the rings may be joined together in a fused fashion. Cycloalkyl groups can contain 3 to 10 atoms in the ring(s) or 3 to 8 atoms in the ring(s). A cycloalkyl group may be unsubstituted or substituted. Typical cycloalkyl groups include, but are in no way limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.

[0028] As used herein, “cycloalkenyl” refers to a mono- or multi-cyclic hydrocarbon ring system that contains one or more double bonds in at least one ring; although, if there is more than one, the double bonds cannot form a fully delocalized pi-electron system throughout all the rings (otherwise the group would be “aryl,” as defined herein). When composed of two or more rings, the rings may be connected together in a fused fashion. A cycloalkenyl can contain 3 to 10 atoms in the ring(s) or 3 to 8 atoms in the ring(s). A cycloalkenyl group may be unsubstituted or substituted.

[0029] As used herein, “aryl” refers to a carbocyclic (all carbon) monocyclic or multicyclic aromatic ring system (including fused ring systems where two carbocyclic rings share a chemical bond) that has a fully delocalized pi-electron system throughout all the rings. The number of carbon atoms in an aryl group can vary. For example, the aryl group can be a C₆-C₁₄ aryl group, a C₆-C₁₀ aryl group, or a C₆ aryl group. Examples of aryl groups include, but are not limited to, benzene, naphthalene and azulene. An aryl group may be substituted or unsubstituted.

[0030] As used herein, “heteroaryl” refers to a monocyclic, bicyclic and tricyclic aromatic ring system (a ring system with fully delocalized pi-electron system) that contain(s) one or more heteroatoms (for example, 1 to 5 heteroatoms), that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur. The number of atoms in the ring(s) of a heteroaryl group can vary. For example, the heteroaryl group can contain 4 to 14 atoms in the ring(s), 5 to 10 atoms in the ring(s) or 5 to 6 atoms in the ring(s). Furthermore, the term “heteroaryl” includes fused ring systems where two rings, such as at least one aryl ring and at least one heteroaryl ring, or at least two heteroaryl rings, share at least one chemical bond. Examples of heteroaryl rings include, but are not limited to, furan, furazan, thiophene, benzothiophene, phthalazine, pyrrole, oxazole, benzoxazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, thiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, benzothiazole, imidazole, benzimidazole, indole, indazole, pyrazole, benzopyrazole, isoxazole, benzoisoxazole, isothiazole, triazole, benzotriazole, thiadiazole, tetrazole, pyridine, pyridazine, pyrimidine, pyrazine, purine, pteridine, quinoline, isoquinoline, quinazoline, quinoxaline, cinnoline and triazine. A heteroaryl group may be substituted or unsubstituted.

[0031] As used herein, “heterocyclyl” or “heteroalicyclyl” refers to three-, four-, five-, six-, seven-, eight-, nine-, ten-, up to 18-membered monocyclic, bicyclic and tricyclic ring system wherein carbon atoms together with from 1 to 5 heteroatoms constitute said ring system. A heterocycle may optionally contain one or more unsaturated bonds situated in such a way, however, that a fully delocalized pi-electron system does not occur throughout all the rings. The heteroatom(s) is an element other than carbon including, but not limited to, oxygen, sulfur and nitrogen. A heterocycle may further contain one or more carbonyl or thiocarbonyl functionalities, so as to make the definition include oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates. When composed of two or more rings, the rings may be joined together in a fused fashion. Additionally, any nitrogens in a heteroalicyclic may be quaternized. Heterocyclyl or heteroalicyclic groups may be unsubstituted or substituted. Examples of such “heterocyclyl” or “heteroalicyclyl” groups include but are not limited to, 1,3-dioxin, 1,3-dioxane, 1,4-dioxane, 1,2-dioxolane, 1,3-dioxolane, 1,4-dioxolane, 1,3-oxathiane, 1,4-oxathiin, 1,3-oxathiolane, 1,3-dithiole, 1,3-dithiolane, 1,4-oxathiane, tetrahydro-1,4-thiazine, 2H-1,2-oxazine, maleimide, succinimide, barbituric acid, thiobarbituric acid, dioxopiperazine, hydantoin, dihydrouracil, trioxane, hexahydro-1,3,5-triazine, imidazoline, imidazolidine, isoxazoline, isoxazolidine, oxazoline, oxazolidine, oxazolidinone, thiazoline, thiazolidine, morpholine, oxirane, piperidine N-Oxide, piperidine, piperazine, pyrrolidine, pyrrolidone, pyrrolidione, 4-piperidone, pyrazoline, pyrazolidine, 2-oxopyrrolidine, tetrahydropyran, 4H-pyran, tetrahydrothiopyran, thiamorpholine, thiamorpholine sulfoxide, thiamorpholine sulfone and their benzo-fused analogs (e.g., benzimidazolidinone, tetrahydroquinoline and 3,4-methylenedioxyphenyl).

[0032] As used herein, “aralkyl” and “aryl(alkyl)” refer to an aryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and aryl group of an aryl(alkyl) may be substituted or unsubstituted. Examples include but are not limited to benzyl, 2-phenyl(alkyl), 3-phenyl(alkyl) and naphthyl(alkyl).

[0033] As used herein, “heteroaralkyl” and “heteroaryl(alkyl)” refer to a heteroaryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and heteroaryl group of heteroaralkyl may be substituted or unsubstituted. Examples include but are not limited to 2-thienyl(alkyl), 3-thienyl(alkyl), furyl(alkyl), thienyl(alkyl), pyrrolyl(alkyl), pyridyl(alkyl), isoxazolyl(alkyl), imidazolyl(alkyl) and their benzo-fused analogs.

[0034] A “heteroalicyclyl(alkyl)” and “heterocyclyl(alkyl)” refer to a heterocyclic or a heteroalicyclylic group connected, as a substituent, via a lower alkylene group. The lower alkylene and heterocyclyl of a heteroalicyclyl(alkyl) may be substituted or unsubstituted. Examples include but are not limited tetrahydro-2H-pyran-4-yl(methyl), piperidin-4-yl(ethyl), piperidin-4-yl(propyl), tetrahydro-2H-thiopyran-4-yl(methyl) and 1,3-thiazinan-4-yl(methyl).

[0035] “Lower alkylene groups” are straight-chained —CH₂— tethering groups, forming bonds to connect molecular fragments via their terminal carbon atoms. Examples include but are not limited to methylene (—CH₂—), ethylene (—CH₂CH₂—), propylene (—CH₂CH₂CH₂—) and butylene (—CH₂CH₂CH₂CH₂—). A lower alkylene group can be substituted by replacing one or more hydrogen of the lower alkylene group with a substituent(s) listed under the definition of “substituted.”

[0036] As used herein, “alkoxy” refers to the formula —OR wherein R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl is defined herein. A non-limiting list of alkoxys are methoxy, ethoxy, n-propoxy, 1-methylethoxy (isopropoxy), n-butoxy, iso-butoxy, sec-butoxy, tert-butoxy, phenoxy and benzoxy. An alkoxy may be substituted or unsubstituted.

[0037] As used herein, “acyl” refers to a hydrogen, alkyl, alkenyl, alkynyl, or aryl connected, as substituents, via a carbonyl group. Examples include formyl, acetyl, propanoyl, benzoyl and acryl. An acyl may be substituted or unsubstituted.

[0038] As used herein, “hydroxyalkyl” refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a hydroxy group. Exemplary hydroxyalkyl groups include but are not limited to, 2-hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl and 2,2-dihydroxyethyl. A hydroxyalkyl may be substituted or unsubstituted.

[0039] As used herein, “haloalkyl” refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkyl, di-haloalkyl and tri-haloalkyl). Such groups include but are not limited to, chloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, 1-chloro-2-fluoromethyl and 2-fluoroisobutyl. A haloalkyl may be substituted or unsubstituted.

[0040] As used herein, “haloalkoxy” refers to an —O-alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkoxy, di-haloalkoxy and tri-haloalkoxy). Such groups include but are not limited to, chloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-chloro-2-fluoromethoxy and 2-fluoroisobutoxy. A haloalkoxy may be substituted or unsubstituted.

[0041] A “sulfenyl” group refers to an “—SR” group in which R can be hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. A sulfenyl may be substituted or unsubstituted.

[0042] A “sulfinyl” group refers to an “—S(═O)—R” group in which R can be the same as defined with respect to sulfenyl. A sulfinyl may be substituted or unsubstituted.

[0043] A “sulfonyl” group refers to an “SO₂R” group in which R can be the same as defined with respect to sulfenyl. A sulfonyl may be substituted or unsubstituted.

[0044] An “O-carboxy” group refers to a “RC(═O)O—” group in which R can be hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl, as defined herein. An O-carboxy may be substituted or unsubstituted.

[0045] The terms “ester” and “C-carboxy” refer to a “—C(═O)OR” group in which R can be the same as defined with respect to O-carboxy. An ester and C-carboxy may be substituted or unsubstituted.

[0046] A “thiocarbonyl” group refers to a “—C(═S)R” group in which R can be the same as defined with respect to O-carboxy. A thiocarbonyl may be substituted or unsubstituted.

[0047] A “trihalomethanesulfonyl” group refers to an “X₃CSO₂—” group wherein each X is a halogen.

[0048] A “trihalomethanesulfonamido” group refers to an “X₃CS(O)₂N(R_A)—” group wherein each X is a halogen, and R_A is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl.

[0049] The term “amino” as used herein refers to a —NH₂ group.

[0050] As used herein, the term “hydroxy” refers to a —OH group.

[0051] A “cyano” group refers to a “—CN” group.

[0052] The term “azido” as used herein refers to a —N₃ group.

[0053] An “isocyanato” group refers to a “—NCO” group.

[0054] A “thiocyanato” group refers to a “—CNS” group.

[0055] An “isothiocyanato” group refers to an “—NCS” group.

[0056] A “mercapto” group refers to an “—SH” group.

[0057] A “carbonyl” group refers to a C═O group.

[0058] An “S-sulfonamido” group refers to a “—SO₂N(R_AR_B)” group in which R_A and R_B can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An S-sulfonamido may be substituted or unsubstituted.

[0059] An “N-sulfonamido” group refers to a “RSO₂N(R_A)—” group in which R and R_A can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An N-sulfonamido may be substituted or unsubstituted.

[0060] An “O-carbamyl” group refers to a “—OC(═O)N(R_AR_B)” group in which R_A and R_B can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An O-carbamyl may be substituted or unsubstituted.

[0061] An “N-carbamyl” group refers to an “ROC(═O)N(R_A)—” group in which R and R_A can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An N-carbamyl may be substituted or unsubstituted.

[0062] An “O-thiocarbamyl” group refers to a “—OC(═S)—N(R_AR_B)” group in which R_A and R_B can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An O-thiocarbamyl may be substituted or unsubstituted.

[0063] An “N-thiocarbamyl” group refers to an “ROC(═S)N(R_A)—” group in which R and R_A can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An N-thiocarbamyl may be substituted or unsubstituted.

[0064] A “C-amido” group refers to a “—C(═O)N(R_AR_B)” group in which R_A and R_B can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. A C-amido may be substituted or unsubstituted.

[0065] An “N-amido” group refers to a “RC(═O)N(R_A)—” group in which R and R_A can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), (heteroaryl)alkyl or (heterocyclyl)alkyl. An N-amido may be substituted or unsubstituted.

[0066] The term “halogen atom” or “halogen” as used herein, means any one of the radio-stable atoms of column 7 of the Periodic Table of the Elements, such as, fluorine, chlorine, bromine and iodine.

[0067] Where the numbers of substituents is not specified (e.g. haloalkyl), there may be one or more substituents present. For example “haloalkyl” may include one or more of the same or different halogens. As another example, “C₁-C₃ alkoxyphenyl” may include one or more of the same or different alkoxy groups containing one, two or three atoms.

[0068] As used herein, the abbreviations for any protective groups, amino acids and other compounds, are, unless indicated otherwise, in accord with their common usage, recognized abbreviations, or the IUPAC-IUB Commission on Biochemical Nomenclature (See, Biochem. 11:942-944 (1972)).

[0069] The term “nucleoside” is used herein in its ordinary sense as understood by those skilled in the art, and refers to a compound composed of an optionally substituted pentose moiety or modified pentose moiety attached to a heterocyclic base or tautomer thereof via a N-glycosidic bond, such as attached via the 9-position of a purine-base or the 1-position of a pyrimidine-base. Examples include, but are not limited to, a ribonucleoside comprising a ribose moiety and a deoxyribonucleoside comprising a deoxyribose moiety. A modified pentose moiety is a pentose moiety in which an oxygen atom has been replaced with a carbon and/or a carbon has been replaced with a sulfur or an oxygen atom. A “nucleoside” is a monomer that can have a substituted base and/or sugar moiety. Additionally, a nucleoside can be incorporated into larger DNA and/or RNA polymers and oligomers. In some instances, the nucleoside can be a nucleoside analog drug.

[0070] The term “nucleotide” is used herein in its ordinary sense as understood by those skilled in the art, and refers to a nucleoside having a phosphate ester bound to the pentose moiety, for example, at the 5′-position.

[0071] As used herein, the term “heterocyclic base” refers to an optionally substituted nitrogen-containing heterocyclyl that can be attached to an optionally substituted pentose moiety or modified pentose moiety. In some embodiments, the heterocyclic base can be selected from an optionally substituted purine-base, an optionally substituted pyrimidine-base and an optionally substituted triazole-base (for example, a 1,2,4-triazole). The term “purine-base” is used herein in its ordinary sense as understood by those skilled in the art, and includes its tautomers. Similarly, the term “pyrimidine-base” is used herein in its ordinary sense as understood by those skilled in the art, and includes its tautomers. A non-limiting list of optionally substituted purine-bases includes purine, adenine, guanine, hypoxanthine, xanthine, alloxanthine, 7-alkylguanine (e.g. 7-methylguanine), theobromine, caffeine, uric acid and isoguanine. Examples of pyrimidine-bases include, but are not limited to, cytosine, thymine, uracil, 5,6-dihydrouracil and 5-alkylcytosine (e.g., 5-methylcytosine). An example of an optionally substituted triazole-base is 1,2,4-triazole-3-carboxamide. Other non-limiting examples of heterocyclic bases include diaminopurine, 8-oxo-N⁶-alkyladenine (e.g., 8-oxo-N⁶-methyladenine), 7-deazaxanthine, 7-deazaguanine, 7-deazaadenine, N⁴,N⁴-ethanocytosin, N⁶,N⁶-ethano-2,6-diaminopurine, 5-halouracil (e.g., 5-fluorouracil and 5-bromouracil), pseudoisocytosine, isocytosine, isoguanine, and other heterocyclic bases described in U.S. Pat. Nos. 5,432,272 and 7,125,855, which are incorporated herein by reference for the limited purpose of disclosing additional heterocyclic bases. In some embodiments, a heterocyclic base can be optionally substituted with an amine or an enol protecting group(s).

[0072] The term “—N-linked amino acid” refers to an amino acid that is attached to the indicated moiety via a main-chain amino or mono-substituted amino group. When the amino acid is attached in an —N-linked amino acid, one of the hydrogens that is part of the main-chain amino or mono-substituted amino group is not present and the amino acid is attached via the nitrogen. N-linked amino acids can be substituted or unsubstituted.

[0073] The term “—N-linked amino acid ester derivative” refers to an amino acid in which a main-chain carboxylic acid group has been converted to an ester group. In some embodiments, the ester group has a formula selected from alkyl-O—C(═O)—, cycloalkyl-O—C(═O)—, aryl-O—C(═O)— and aryl(alkyl)-O—C(═O)—. A non-limiting list of ester groups include substituted and unsubstituted versions of the following: methyl-O—C(═O)—, ethyl-O—C(═O)—, n-propyl-O—C(═O)—, isopropyl-O—C(═O)—, n-butyl-O—C(═O)—, isobutyl-O—C(═O)—, tert-butyl-O—C(═O)—, neopentyl-O—C(═O)—, cyclopropyl-O—C(═O)—, cyclobutyl-O—C(═O)—, cyclopentyl-O—C(═O)—, cyclohexyl-O—C(═O)—, phenyl-O—C(═O)—, benzyl-O—C(═O)— and naphthyl-O—C(═O)—. N-linked amino acid ester derivatives can be substituted or unsubstituted.

[0074] The term “—O-linked amino acid” refers to an amino acid that is attached to the indicated moiety via the hydroxy from its main-chain carboxylic acid group. When the amino acid is attached in an —O-linked amino acid, the hydrogen that is part of the hydroxy from its main-chain carboxylic acid group is not present and the amino acid is attached via the oxygen. O-linked amino acids can be substituted or unsubstituted.

[0075] As used herein, the term “amino acid” refers to any amino acid (both standard and non-standard amino acids), including, but not limited to, α-amino acids, β-amino acids, γ-amino acids and δ-amino acids. Examples of suitable amino acids include, but are not limited to, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan and valine. Additional examples of suitable amino acids include, but are not limited to, ornithine, hypusine, 2-aminoisobutyric acid, dehydroalanine, gamma-aminobutyric acid, citrulline, beta-alanine, alpha-ethyl-glycine, alpha-propyl-glycine and norleucine.

[0076] The terms “phosphorothioate” and “phosphothioate” refer to a compound of the general formula

its protonated forms (for example,

and its tautomers (such as

[0077] As used herein, the term “phosphate” is used in its ordinary sense as understood by those skilled in the art, and includes its protonated forms (for example,

[0078] As used herein, the terms “monophosphate,” “diphosphate,” and “triphosphate” are used in their ordinary sense as understood by those skilled in the art, and include protonated forms.

[0079] The terms “protecting group” and “protecting groups” as used herein refer to any atom or group of atoms that is added to a molecule in order to prevent existing groups in the molecule from undergoing unwanted chemical reactions. Examples of protecting group moieties are described in T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3. Ed. John Wiley & Sons, 1999, and in J. F. W. McOmie, Protective Groups in Organic Chemistry Plenum Press, 1973, both of which are hereby incorporated by reference for the limited purpose of disclosing suitable protecting groups. The protecting group moiety may be chosen in such a way, that they are stable to certain reaction conditions and readily removed at a convenient stage using methodology known from the art. A non-limiting list of protecting groups include benzyl; substituted benzyl; alkylcarbonyls and alkoxycarbonyls (e.g., t-butoxycarbonyl (BOC), acetyl, or isobutyryl); arylalkylcarbonyls and arylalkoxycarbonyls (e.g., benzyloxycarbonyl); substituted methyl ether (e.g. methoxymethyl ether); substituted ethyl ether; a substituted benzyl ether; tetrahydropyranyl ether; silyls (e.g., trimethylsilyl, triethylsilyl, triisopropylsilyl, t-butyldimethylsilyl, tri-iso-propylsilyloxymethyl, [2-(trimethylsilyl)ethoxy]methyl or t-butyldiphenylsilyl); esters (e.g. benzoate ester); carbonates (e.g. methoxymethylcarbonate); sulfonates (e.g. tosylate or mesylate); acyclic ketal (e.g. dimethyl acetal); cyclic ketals (e.g., 1,3-dioxane, 1,3-dioxolanes and those described herein); acyclic acetal; cyclic acetal (e.g., those described herein); acyclic hemiacetal; cyclic hemiacetal; cyclic dithioketals (e.g., 1,3-dithiane or 1,3-dithiolane); orthoesters (e.g., those described herein) and triarylmethyl groups (e.g., trityl; monomethoxytrityl (MMTr); 4,4′-dimethoxytrityl (DMTr); 4,4′,4″-trimethoxytrityl (TMTr); and those described herein).

[0080] The term “pharmaceutically acceptable salt” refers to a salt of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound. In some embodiments, the salt is an acid addition salt of the compound. Pharmaceutical salts can be obtained by reacting a compound with inorganic acids such as hydrohalic acid (e.g., hydrochloric acid or hydrobromic acid), sulfuric acid, nitric acid and phosphoric acid. Pharmaceutical salts can also be obtained by reacting a compound with an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids, for example formic, acetic, succinic, lactic, malic, tartaric, citric, ascorbic, nicotinic, methanesulfonic, ethanesulfonic, p-toluenesulfonic, salicylic or naphthalenesulfonic acid. Pharmaceutical salts can also be obtained by reacting a compound with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, C₁-C₇ alkylamine, cyclohexylamine, triethanolamine, ethylenediamine, and salts with amino acids such as arginine and lysine.

[0081] Terms and phrases used in this application, and variations thereof, especially in the appended claims, unless otherwise expressly stated, should be construed as open ended as opposed to limiting. As examples of the foregoing, the term ‘including’ should be read to mean ‘including, without limitation,’ ‘including but not limited to,’ or the like; the term ‘comprising’ as used herein is synonymous with ‘including,’ ‘containing,’ or ‘characterized by,’ and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps; the term ‘having’ should be interpreted as ‘having at least;’ the term ‘includes’ should be interpreted as ‘includes but is not limited to;’ the term ‘example’ is used to provide exemplary instances of the item in discussion, not an exhaustive or limiting list thereof; and use of terms like ‘preferably,’ ‘preferred,’ ‘desired,’ or ‘desirable,’ and words of similar meaning should not be understood as implying that certain features are critical, essential, or even important to the structure or function, but instead as merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment. In addition, the term “comprising” is to be interpreted synonymously with the phrases “having at least” or “including at least”. When used in the context of a process, the term “comprising” means that the process includes at least the recited steps, but may include additional steps. When used in the context of a compound, composition or device, the term “comprising” means that the compound, composition or device includes at least the recited features or components, but may also include additional features or components. Likewise, a group of items linked with the conjunction ‘and’ should not be read as requiring that each and every one of those items be present in the grouping, but rather should be read as ‘and/or’ unless expressly stated otherwise. Similarly, a group of items linked with the conjunction ‘or’ should not be read as requiring mutual exclusivity among that group, but rather should be read as ‘and/or’ unless expressly stated otherwise.

[0082] With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity. The indefinite article “a” or “an” does not exclude a plurality. A single processor or other unit may fulfill the functions of several items recited in the claims. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.

[0083] It is understood that, in any compound described herein having one or more chiral centers, if an absolute stereochemistry is not expressly indicated, then each center may independently be of R-configuration or S-configuration or a mixture thereof. Thus, the compounds provided herein may be enantiomerically pure, enantiomerically enriched, racemic mixture, diastereomerically pure, diastereomerically enriched, or a stereoisomeric mixture. In addition it is understood that, in any compound described herein having one or more double bond(s) generating geometrical isomers that can be defined as E or Z, each double bond may independently be E or Z a mixture thereof.

[0084] Likewise, it is understood that, in any compound described, all tautomeric forms are also intended to be included. For example all tautomers of a phosphate and a phosphorothioate groups are intended to be included. Examples of tautomers of a phosphorothioate include the following:

Furthermore, all tautomers of heterocyclic bases known in the art are intended to be included, including tautomers of natural and non-natural purine-bases and pyrimidine-bases.

[0085] It is to be understood that where compounds disclosed herein have unfilled valencies, then the valencies are to be filled with hydrogens or isotopes thereof, e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).

[0086] It is understood that the compounds described herein can be labeled isotopically. Substitution with isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements. Each chemical element as represented in a compound structure may include any isotope of said element. For example, in a compound structure a hydrogen atom may be explicitly disclosed or understood to be present in the compound. At any position of the compound that a hydrogen atom may be present, the hydrogen atom can be any isotope of hydrogen, including but not limited to hydrogen-1 (protium) and hydrogen-2 (deuterium). Thus, reference herein to a compound encompasses all potential isotopic forms unless the context clearly dictates otherwise.

[0087] It is understood that the methods and combinations described herein include crystalline forms (also known as polymorphs, which include the different crystal packing arrangements of the same elemental composition of a compound), amorphous phases, salts, solvates and hydrates. In some embodiments, the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol, or the like. In other embodiments, the compounds described herein exist in unsolvated form. Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and may be formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol, or the like. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is alcohol. In addition, the compounds provided herein can exist in unsolvated as well as solvated forms. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein.

[0088] Where a range of values is provided, it is understood that the upper and lower limit, and each intervening value between the upper and lower limit of the range is encompassed within the embodiments.

[0089] Some embodiments disclosed herein relate to a compound of Formula (I), or a pharmaceutically acceptable salt thereof:

wherein: B¹ can be selected from an optionally substituted

an optionally substituted

and an optionally substituted

-------- can be absent or a single bond; when is -------- a single bond, then R^P can be

and R⁴ can be O; when -------- is absent, then R^P can be hydrogen or

and R⁴ can be —OH or F; R¹ can be selected from an —O-optionally substituted aryl,

O⁻, and —OH; R² can be selected from O⁻, —OH, an optionally substituted N-linked amino acid, an optionally substituted N-linked amino acid ester derivative and

provided that when R² is O⁻ or —OH, R¹ is selected from

[0090] R³, each R⁶ and R⁷ can be independently hydrogen or deuterium; R⁵ can be —OH or F; R⁸, R⁹ and R¹⁰ can be independently absent or hydrogen; B^1A, B^2A, B^3A and B^4A can be independently hydrogen or deuterium; B^5A can be —O-optionally substituted C_1-6 alkyl or —NH₂, R^p1 can be selected from O⁻, OH, an —O-optionally substituted C_1-6 alkyl, an —O-optionally substituted aryl,

an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative; R^p1, R^p3, R^p5 and R^p6 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl and an optionally substituted aryl; R^p4 and R^p7 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl, an optionally substituted aryl, an optionally substituted —O—C_1-24 alkyl, an optionally substituted —O-aryl, an optionally substituted —O-heteroaryl and an optionally substituted —O-monocyclic heterocyclyl; R^p8 and R^p9 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl and an optionally substituted aryl; n can be 0 or 1; r can be 1 or 2; u can be 3, 4, or 5; and Z^p1 can be O or S.

[0091] In some embodiments, -------- can be absent, R^P can be

and R⁴ can be —OH or F, and the compound of Formula (I) can have the structure of Formula (II), or a pharmaceutically acceptable salt thereof:

wherein: B¹, R¹, R², R³, R⁴, R⁵, each R⁶ and R⁷ are provided herein.

[0092] A variety of groups can be attached to the phosphorus atom of

In some embodiments, R¹ can be an —O-optionally substituted aryl. For example, R¹ can be an —O-optionally substituted phenyl. When the phenyl is substituted, the ring can be substituted 1, 2, 3 or more than 3 times. Suitable mono-substituted phenyl groups include, ortho-substituted phenyl, meta-substituted phenyl and para-substituted phenyl. In some embodiments, R¹ can be an —O-unsubstituted aryl. In some embodiments, R¹ can be an —O-optionally substituted naphthyl. In some embodiments, R¹ can be an —O-unsubstituted phenyl. In some embodiments, R¹ can be an —O-unsubstituted naphthyl.

[0093] In some embodiments, R² can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative. Various amino acids are suitable, including those described herein. Examples of suitable amino acids include, but are not limited to, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine. In other embodiments, R² can be an optionally substituted N-linked amino acid ester derivative. Examples of suitable amino acid ester derivatives include, but are not limited to, an ester derivative of any of the following amino acids, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine. Additional examples of N-linked amino acid ester derivatives include, but are not limited to, an ester derivative of any of the following amino acids: alpha-ethyl-glycine, alpha-propyl-glycine and beta-alanine. In some embodiments, the N-linked amino acid ester derivative can be selected from alanine isopropyl ester, alanine cyclohexyl ester, alanine neopentyl ester, valine isopropyl ester, isoleucine isopropyl ester, methionine isopropyl ester and leucine isopropyl ester.

[0094] In some embodiments, R² can be

wherein R¹¹ can be selected from hydrogen, an optionally substituted C_1-6-alkyl, an optionally substituted C_3-6 cycloalkyl, an optionally substituted aryl, an optionally substituted aryl(C_1-6 alkyl) and an optionally substituted haloalkyl; R¹² can be selected from hydrogen, an optionally substituted C_1-6 alkyl, an optionally substituted C_1-6 haloalkyl, an optionally substituted C_3-6 cycloalkyl, an optionally substituted C₆ aryl, an optionally substituted C₁₀ aryl and an optionally substituted aryl(C_1-6 alkyl); and R¹³ can be hydrogen or an optionally substituted C_1-4-alkyl; or R¹² and R¹³ are taken together to form an optionally substituted C_3-6 cycloalkyl.

[0095] In some embodiments, R¹² can be substituted by a variety of substituents. Suitable examples of substituents include, but are not limited to, N-amido, mercapto, alkylthio, an optionally substituted aryl, hydroxyl, an optionally substituted heteroaryl, O-carboxy and amino. In some embodiments R¹² can be hydrogen. In some embodiments, R¹² can be an optionally substituted C_1-6-alkyl. In some embodiments, R¹³ can be hydrogen. In some embodiments R¹³ can be an optionally substituted C_1-4 alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or tert-butyl. In some embodiments R¹³ can be methyl. In some embodiments, R¹¹ can be an optionally substituted C_1-6 alkyl. Examples of optionally substituted C_1-6-alkyls include optionally substituted variants of the following: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) and hexyl (branched and straight-chained). In some embodiments, R¹¹ can be methyl or isopropyl. In some embodiments, R¹¹ can be ethyl or neopentyl. In some embodiments, R¹¹ can be an optionally substituted C_3-6 cycloalkyl. Examples of optionally substituted C_3-6 cycloalkyls include optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Depending on the groups that are selected for R¹² and R¹³, the carbon to which R¹² and R¹³ are attached may be a chiral center. In some embodiments, the carbon to which R¹² and R¹³ are attached may be a (R)-chiral center. In other embodiments, the carbon to which R¹² and R¹³ are attached may be a (S)-chiral center.

[0096] Examples of suitable

groups include the following:

[0097] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be a phosphoramidate prodrug. For example, R¹ can be an —O-optionally substituted aryl, and R² can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative.

[0098] In some embodiments, R¹ and/or R² can be

In some embodiments R¹ and R² can both be a isopropyloxycarbonyloxymethoxy (POC) group, and form a bis(POC) prodrug.

[0099] In some embodiments, R¹ and R² can independently be O⁻ or —OH, and a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be a monophosphate. In other embodiments, R¹ can be

wherein R⁸, R⁹ and R¹⁰ can be independently absent or hydrogen, n can be 0 and R² can be O⁻ or —OH. Those skilled in the art understand that when R⁸, R⁹ and/or R¹⁰ are absent, the associated oxygen can have a negative charge. For example, when R⁹ is absent, then the associated oxygen can have a negative charge, such that R¹ can be

[0100]

R⁹ and R¹⁰ are independently absent or hydrogen, n is 0 and R² is O⁻ or —OH, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be a diphosphate. In yet other embodiments R¹ can be

wherein R⁸, R⁹ and R¹⁰ can be independently absent or hydrogen, n can be 1 and R² can be O⁻ or —OH. When R¹ is

R⁸, R⁹ and R¹⁰ are independently absent or hydrogen, n is 1 and R² is O⁻ or —OH, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be a triphosphate.

[0101] In some embodiments of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt of the foregoing, R⁴ is —OH. In other embodiments, R⁴ is F.

[0102] In some embodiments of Formula (I), -------- can be a single bond, R^P can be

and R⁴ can be O, and the compound of Formula (I) can have the structure of Formula (III), or a pharmaceutically acceptable salt thereof:

wherein: B¹, R³, R⁵, each R⁶, R⁷ and R^p1 are provided herein.

[0103] In some embodiments, R^p1 can be O⁻. In other embodiments, R^p1 can be OH. In other embodiments, R^p1 can be an —O-optionally substituted C_1-6 alkyl. For example, R^p1 can be a substituted or an unsubstituted version of the following: methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, tert-butoxy, pentoxy (branched or straight chained) and hexoxy (branched or straight chained).

[0104] In some embodiments, R^p1 can be an —O-optionally substituted aryl. For example, R^p1 can be an —O-optionally substituted phenyl. When the phenyl is substituted, the ring can be substituted 1, 2, 3 or more than 3 times. Suitable mono-substituted phenyl groups include ortho-substituted phenyl, meta-substituted phenyl and para-substituted phenyl. In some embodiments, R^p1 can be an —O-unsubstituted aryl. In some embodiments, R^p1 can be an —O-optionally substituted naphthyl. In some embodiments, R^p1 can be an —O-unsubstituted phenyl. In some embodiments, R^p1 can be an —O-unsubstituted naphthyl.

[0105] In some embodiments, R^p1 can be

wherein R^p1 and R^p3 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl and an optionally substituted aryl; and R^p4 can be selected from hydrogen, an optionally substituted C_1-24 alkyl, an optionally substituted aryl, an optionally substituted —O—C_1-24 alkyl, an optionally substituted —O-aryl, an optionally substituted —O-heteroaryl and an optionally substituted —O-monocyclic heterocyclyl. In some embodiments, at least one of R^p2 and R^p3 can be hydrogen. In other embodiments, both R^p2 and R^p3 can be hydrogen. In other embodiments, at least one of R^p2 and R^p3 can be an optionally substituted C_1-24 alkyl or an optionally substituted aryl. In some embodiments, R^p4 can be an optionally substituted C_1-24 alkyl. In some embodiments, R^p4 can be an unsubstituted C_1-4 alkyl. In other embodiments, R^p4 can be an optionally substituted aryl. In still other embodiments, R^p4 can be an optionally substituted —O—C_1-24 alkyl, an optionally substituted —O-aryl, an optionally substituted —O-heteroaryl or an optionally substituted —O-monocyclic heterocyclyl. In some embodiments, R^p4 can be an unsubstituted —O—C_1-4 alkyl.

[0106] In some embodiments, R^p1 can be

wherein R^p5 and R^p6 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl and an optionally substituted aryl; R^p7 can be independently selected from hydrogen, an optionally substituted C_1-24 alkyl, an optionally substituted aryl, an optionally substituted —O—C_1-24 alkyl, an optionally substituted —O-aryl, an optionally substituted —O-heteroaryl and an optionally substituted —O-monocyclic heterocyclyl; and Z^p1 can be independently O (oxygen) or S (sulfur). In some embodiments, at least one of R^p5 and R^p6 can be hydrogen. In other embodiments, both R^p5 and R^p6 can be hydrogen. In other embodiments, at least one of R^p5 and R^p6 can be an optionally substituted C_1-24 alkyl or an optionally substituted aryl. In some embodiments, R^p7 can be an optionally substituted C_1-24 alkyl. In some embodiments, R^p7 can be an unsubstituted C_1-4 alkyl. In other embodiments, R^p7 can be an optionally substituted aryl. In still other embodiments, R^p7 can be an optionally substituted —O—C_1-24 alkyl, an optionally substituted —O-aryl, an optionally substituted —O-heteroaryl or an optionally substituted —O-monocyclic heterocyclyl. In some embodiments, R^p7 can be an unsubstituted —O—C_1-4 alkyl. In some embodiments, Z^p1 can be O (oxygen). In other embodiments, Z^p1 can be or S (sulfur). In some embodiments, R^p1 can be isopropyloxycarbonyloxymethyloxy (POC) group. In some embodiments, R^p1 can be pivaloyloxymethyloxy (POM) group.

[0107] In some embodiments, R^p1 can be

In some embodiments, R^p8 can be hydrogen. In other embodiments, R^p8 can be an optionally substituted C_1-24 alkyl. In still other embodiments, R^p8 can be an optionally substituted aryl. In some embodiments, R^p8 can be a C_1-6 alkyl, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained), and hexyl (branched and straight-chained). In some embodiments, r can be 1. In other embodiments, r can be 2.

[0108] In some embodiments, R^p1 can be

In some embodiments, R^p9 can be hydrogen. In other embodiments, R^p9 can be an optionally substituted C_1-24 alkyl. In still other embodiments, R^p9 can be an optionally substituted aryl, for example, an optionally substituted phenyl. In some embodiments, R^p9 can be an optionally substituted C_1-6 alkyl. In some embodiments, R^P9 can be an unsubstituted C_1-6 alkyl. In some embodiments, u can be 3. In other embodiments, u can be 4. In still other embodiments, u can be 5. In some embodiments, R^p1 can be a S-acylthioethoxy (SATE) group and form a SATE ester prodrug.

[0109] In some embodiments, R^p1 can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative. For example, R^p1 can be optionally substituted version of the following: alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, valine and ester derivatives thereof. In some embodiments, R^p1 can be selected from N-alanine isopropyl ester, N-alanine cyclohexyl ester, N-alanine neopentyl ester, N-valine isopropyl ester and N-leucine isopropyl ester. In some embodiments, R^p1 can have the structure

wherein R^p10 can be selected from hydrogen, an optionally substituted C_1-6-alkyl, an optionally substituted C_3-6 cycloalkyl, an optionally substituted aryl, an optionally substituted aryl(C_1-6 alkyl) and an optionally substituted haloalkyl; R^p11 can be selected from hydrogen, an optionally substituted C_1-6 alkyl, an optionally substituted C_1-6 haloalkyl, an optionally substituted C_3-6 cycloalkyl, an optionally substituted C₆ aryl, an optionally substituted C₁₀ aryl and an optionally substituted aryl(C_1-6 alkyl); and R^p12 can be hydrogen or an optionally substituted C_1-4-alkyl; or R^p11 and R^p12 can be taken together to form an optionally substituted C_3-6 cycloalkyl.

[0110] When R^p11 is substituted, R^p11 can be substituted with one or more substituents selected from N-amido, mercapto, alkylthio, an optionally substituted aryl, hydroxy, an optionally substituted heteroaryl, O-carboxy, and amino. In some embodiments, R^p11 can be an unsubstituted C_1-6-alkyl, such as those described herein. In some embodiments, R^p11 can be hydrogen. In other embodiments, R^p11 can be methyl. In some embodiments, R^p10 can be an optionally substituted C_1-6 alkyl. Examples of optionally substituted C_1-6-alkyls include optionally substituted variants of the following: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained), and hexyl (branched and straight-chained). In some embodiments, R^p10 can be methyl or isopropyl. In some embodiments, R^p10 can be ethyl or neopentyl. In other embodiments, R^p10 can be an optionally substituted C_3-6 cycloalkyl. Examples of optionally substituted C_3-6 cycloalkyl include optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. In some embodiments, R^p10 can be an optionally substituted cyclohexyl. In still other embodiments, R^p10 can be an optionally substituted aryl, such as phenyl and naphthyl. In yet still other embodiments, R^p10 can be an optionally substituted aryl(C_1-6 alkyl). In some embodiments, R^p10 can be an optionally substituted benzyl. In some embodiments, R^p10 can be an optionally substituted C_1-6 haloalkyl, for example, CF₃. In some embodiments, R^p12 can be hydrogen. In other embodiments, R^p12 can be an optionally substituted C_1-4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl and tert-be taken together to form an optionally substituted C_3-6 cycloalkyl. Examples of optionally substituted C_3-6 cycloalkyl include optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. Depending on the groups that are selected for R^p11 and R^p12, the carbon to which R^p11 and R^p12 are attached may be a chiral center. In some embodiment, the carbon to which R^p11 and R^p12 are attached may be a (R)-chiral center. In other embodiments, the carbon to which R^p11 and R^p12 are attached may be a (S)-chiral center.

[0111] Examples of suitable

groups include the following:

[0112] The R³ attached to the 3′-carbon of the pentose ring of a compound described herein can vary. In some embodiments, R³ can be hydrogen. In other embodiments, R³ can be deuterium.

[0113] Likewise, various substituents can be attached at the 2′-carbon of the pentose ring. In some embodiments R⁵ can be —OH. In other embodiments, R⁵ can be F.

[0114] In some embodiments, at least one R⁶ substituent of the 2′-methyl group can be hydrogen. In other embodiments, at least two R⁶ can be hydrogen. In yet other embodiments, each R⁶ can be hydrogen. In some embodiments, at least one R⁶ can be deuterium. In other embodiments, at least two R⁶ can be deuterium. In yet other embodiments, each R⁶ can be deuterium.

[0115] In some embodiments, R⁷ can be hydrogen. In other embodiments, R⁷ can be deuterium.

[0116] The nucleobase of a compound described herein can vary. In some embodiments, the nucleobase can be an optionally substituted deuterated nucleobase. For example, B¹ can be an optionally deuterated uracil. In some embodiments B¹ can be an optionally substituted

In some embodiments at least one of B^1A and B^2A can be hydrogen. In some embodiments, both B^1A and B^2A can be hydrogen. In other embodiments, at least one of B^1A and B^2A can be deuterium. In yet other embodiments, both B^1A and B^2A can be deuterium.

[0117] In some embodiments, B can be an optionally deuterated guanine or a 6-oxygen protected guanine. For example, B¹ can be an optionally substituted

In some embodiments, B^3A can be hydrogen. In other embodiments, B^3A can be deuterium. In other embodiments, B¹ can be an optionally substituted

wherein B^5A can be an —O-optionally substituted C_1-6 alkyl. In some embodiments of this paragraph, B^4A can be hydrogen. In other embodiments of this paragraph, B^4A can be deuterium. In some embodiments, B^5A can be an optionally substituted methoxy, an optionally substituted ethoxy, an optionally substituted n-propyloxy, an optionally substituted isopropyloxy, an optionally substituted n-butyloxy, an optionally substituted isobutyloxy, an optionally substituted tert-butyloxy, an optionally substituted pentyloxy (branched and straight-chained) or an optionally substituted hexyloxy (branched and straight-chained). In some embodiments, B^5A can be —OCH₂CH₃.

[0118] In some embodiments, B can be an optionally deuterated 2,6-diaminopurine. In some embodiments, B¹ can be an optionally substituted

wherein B^5A can be —NH₂. In some embodiments of this paragraph, B^4A can be hydrogen. In other embodiments of this paragraph, B^4A can be deuterium.

[0119] Examples of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include the following:

[0120] Additional examples of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include the following:

TABLE 1
Formula No.	Structure
Ia
Ib
Ic

[0121] In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, R³ can be hydrogen. In other embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, R³ can be deuterium. In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, each R⁶ can independently be hydrogen or deuterium. In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, at least one R⁶ can be hydrogen. In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, at least two R⁶ can be hydrogen. In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, each R⁶ can be hydrogen. In other embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, at least one R⁶ can be deuterium. In yet other embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, at least two R⁶ can be deuterium. In yet other embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, each R⁶ can be deuterium. In some embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, R⁷ can be hydrogen. In other embodiments of Formulae (Ia), (Ib) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, R⁷ can be deuterium. In some embodiments of Formulae (Ia) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, B^4A can be hydrogen. In other embodiments of Formulae (Ia) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, B^4A can be deuterium. In some embodiments of Formulae (Ia) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, B^5A can be an —O-optionally substituted alkyl. In other embodiments of Formulae (Ia) and/or (Ic), or a pharmaceutically acceptable salt of the foregoing, B^5A can be —NH₂. In some embodiments of Formula (Ib), or a pharmaceutically acceptable salt thereof, at least one of B^1A and B^2A can be hydrogen. In other embodiments of Formula (Ib), or a pharmaceutically acceptable salt thereof, both B^1A and B^2A can be hydrogen. In other embodiments of Formula (Ib), or a pharmaceutically acceptable salt thereof, at least one of B^1A and B^2A can be deuterium. In yet other embodiments of Formula (Ib), or a pharmaceutically acceptable salt thereof, both B^1A and B^2A can be deuterium.

[0122] Further examples of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include:

TABLE 2
Formula No.	Structure
Id
Ie
If
Ig
Ih
Ii
Ij
Ik
Il
Im
In
Io
Ip
Iq
Ir
Is
It
Iu
Iv
Iw
Ix
Iy
Iz
Iaa
Ibb
Icc
Idd
Iee

[0123] In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, R³ can be hydrogen. In other embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, R³ can be deuterium. In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, each R⁶ can independently be hydrogen or deuterium. In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, at least one R⁶ can be hydrogen. In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, at least two R⁶ can be hydrogen. In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, each R⁶ can be hydrogen. In other embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, at least one R⁶ can be deuterium. In yet other embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, at least two R⁶ can be deuterium. In yet other embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, each R⁶ can be deuterium. In some embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, R⁷ can be hydrogen. In other embodiments of the Formulae in Table 2, or a pharmaceutically acceptable salt of the foregoing, R⁷ can be deuterium. In some embodiments of Formulae (Ic), (Il), (Iu), (Iw), (Iy), (Iz), (Iaa), (Ibb), (Icc) and/or (Iee), B^4A can be hydrogen. In other embodiments of Formulae (Ik), (Il), (Iu), (Iw), (Iy), (Iz), (Iaa), (Ibb), (Icc) and/or (Iee), B^4A can be deuterium. In some embodiments of Formulae (Ik), (Il), (Iu), (Iw), (Iy), (Iz), (Iaa), (Ibb), (Icc) and/or (Iee), or a pharmaceutically acceptable salt of the foregoing, B^5A can be an —O-optionally substituted alkyl. In other embodiments of Formulae (Ik), (Il), (Iu), (Iw), (Iy), (Iz), (Iaa), (Ibb), (Icc) and/or (Tee), or a pharmaceutically acceptable salt of the foregoing, B^5A can be —NH₂. In some embodiments of Formulae (Id), (Ig), (Ih), (Ii), (Ij), (Im), (Io), (Ip), (Iq), (Ir), (Is) and (It), or a pharmaceutically acceptable salt of the foregoing, at least one of B^1A and B^2A can be hydrogen. In other embodiments of Formulae (Id), (Ig), (Ih), (Ii), (Ij), (Im), (Io), (Ip), (Iq), (Ir), (Is) and (It), or a pharmaceutically acceptable salt of the foregoing, both B^1A and B^2A can be hydrogen. In still other embodiments of Formulae (Id), (Ig), (Ih), (Ii), (Ij), (Im), (Io), (Ip), (Iq), (Ir), (Is) and (It), or a pharmaceutically acceptable salt of the foregoing, at least one of B^1A and B^2A can be deuterium. In yet other embodiments of Formulae (Id), (Ig), (Ih), (Ii), (Ij), (Im), (Io), (Ip), (Iq), (Ir), (Is) and (It), or a pharmaceutically acceptable salt of the foregoing, both B^1A and B^2A can be deuterium. In some embodiments of Formulae (Ie), (If), (In), (Iv) and (Idd), or a pharmaceutically acceptable salt of the foregoing, B^3A can be hydrogen. In some embodiments of Formulae (Ie), (If), (In), (Iv) and (Idd), or a pharmaceutically acceptable salt of the foregoing, B^3A can be deuterium.

[0124] It will be appreciated by one of ordinary skill in the art that the structures of Formulae (Ia)-(Idd), or a pharmaceutically acceptable salt of the foregoing can be prepared in a similar manner to the preparation of their respective non-deuterated analogs as described in PCT Publication No. WO 2014/100505, which is hereby incorporated by reference in its entirety.

[0125] As described herein, any position of Formula (I), or pharmaceutically acceptable salt thereof, as well as a compounds of Formulae (Ia)-(Idd) that is hydrogen can be replaced with an isotope of hydrogen, such as hydrogen-2 (deuterium). Some embodiments of Formula (I), or a pharmaceutically acceptable salt thereof, are provided in each row of Table 3.

TABLE 3
RP	R1	R2	R4	R5	B1	R3	(R6)3	R7	B1A	B2A	B3A	B4A	B5A
PA	Ph	N-AA	OH	OH	U1	H	HHH	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHH	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HHD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	HDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	H	DDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHH	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HHD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	HDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	U1	D	DDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	H	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	D	H	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	H	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	D	H	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	H	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	D	D	H	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHH	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HHD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	HDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	H	DDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	H	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHH	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HHD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	HDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	F	U1	D	DDD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	H	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	D	H	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	H	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	D	H	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	H	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	D	D	H	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHH	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HHD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	HDD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	H	DDD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	H	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHH	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HHD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	HDD	D	D	D	—	—	—
PA	Ph	N-AA	F	OH	U1	D	DDD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	H	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	D	H	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	H	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	D	H	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	H	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	D	D	H	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHH	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HHD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	HDD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	H	DDD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	H	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHH	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HHD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	HDD	D	D	D	—	—	—
PA	Ph	N-AA	F	F	U1	D	DDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHH	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HHD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	HDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	H	DDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHH	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HHD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	HDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	OH	U1	D	DDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	H	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	D	H	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	H	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	D	H	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	H	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	D	D	H	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHH	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HHD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	HDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	H	DDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	H	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHH	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HHD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	HDD	D	D	D	—	—	—
PA	Naph	N-AA	OH	F	U1	D	DDD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	H	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	D	H	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	H	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	D	H	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	H	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	D	D	H	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHH	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HHD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	HDD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	H	DDD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	H	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHH	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HHD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	HDD	D	D	D	—	—	—
PA	Naph	N-AA	F	OH	U1	D	DDD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	H	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	D	H	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	H	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	D	H	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	H	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	D	D	H	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHH	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HHD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	HDD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	H	DDD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	H	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHH	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HHD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	HDD	D	D	D	—	—	—
PA	Naph	N-AA	F	F	U1	D	DDD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	H	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	D	H	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	H	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	D	H	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	H	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	D	D	H	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHH	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HHD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	HDD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	H	DDD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	H	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHH	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HHD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	HDD	D	D	D	—	—	—
PA	POC	POC	OH	OH	U1	D	DDD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	H	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	D	H	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	H	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	D	H	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	H	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	D	D	H	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHH	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HHD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	HDD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	H	DDD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	H	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHH	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HHD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	HDD	D	D	D	—	—	—
PA	POC	POC	OH	F	U1	D	DDD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	H	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	D	H	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	H	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	D	H	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	H	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	D	D	H	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHH	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HHD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	HDD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	H	DDD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	H	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHH	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HHD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	HDD	D	D	D	—	—	—
PA	POC	POC	F	OH	U1	D	DDD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HHH	H	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HHD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HDD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	H	DDD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HHH	D	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HHD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HDD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	H	DDD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HHH	H	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HHD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HDD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	D	DDD	H	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HHH	D	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HHD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	D	HDD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	D	DDD	D	H	H	—	—	—
PA	POC	POC	F	F	U1	H	HHH	H	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HHD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HDD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	H	DDD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HHH	D	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HHD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HDD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	H	DDD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HHH	H	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HHD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HDD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	D	DDD	H	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HHH	D	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HHD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	D	HDD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	D	DDD	D	H	D	—	—	—
PA	POC	POC	F	F	U1	H	HHH	H	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HHD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HDD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	H	DDD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HHH	D	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HHD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HDD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	H	DDD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HHH	H	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HHD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HDD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	D	DDD	H	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HHH	D	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HHD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	D	HDD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	D	DDD	D	D	H	—	—	—
PA	POC	POC	F	F	U1	H	HHH	H	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HHD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HDD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	H	DDD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HHH	D	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HHD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	H	HDD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	H	DDD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HHH	H	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HHD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HDD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	D	DDD	H	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HHH	D	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HHD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	D	HDD	D	D	D	—	—	—
PA	POC	POC	F	F	U1	D	DDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHH	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HHD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	HDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	H	DDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHH	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HHD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	HDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	OH	U1	D	DDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	H	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	D	H	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	H	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	D	H	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	H	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	D	D	H	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHH	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HHD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	HDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	H	DDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	H	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHH	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HHD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	HDD	D	D	D	—	—	—
PA	P1	OH/O−	OH	F	U1	D	DDD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	D	H	H	—	—	—
PA	P1	OH/	F	OH	U1	H	HHD	D	H	H	—	—	—
		O−
PA	P1	OH/O−	F	OH	U1	H	HDD	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	H	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	D	H	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	H	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	D	H	D	—	—	—
PA	P1	OH/	F	OH	U1	D	HDD	D	H	D	—	—	—
		O−
PA	P1	OH/O−	F	OH	U1	D	DDD	D	H	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	H	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	D	D	H	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHH	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HHD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	HDD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	H	DDD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	H	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHH	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HHD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	HDD	D	D	D	—	—	—
PA	P1	OH/O−	F	OH	U1	D	DDD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	H	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	D	H	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	H	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	D	H	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	H	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	D	D	H	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHH	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HHD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	HDD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	H	DDD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	H	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHH	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HHD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	HDD	D	D	D	—	—	—
PA	P1	OH/O−	F	F	U1	D	DDD	D	D	D	—	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHH	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	DDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHH	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	DDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHH	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	DDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHH	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	HDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	D	DDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHH	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	HDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	DDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHH	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	HHD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	HDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	H	DDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHH	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	DDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHH	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HHD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	HDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G1	D	DDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HHH	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HHD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	DDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HHH	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HHD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	DDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HHH	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HHD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	DDD	H	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HHH	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HHD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	HDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	D	DDD	D	—	—	H	—	—
PA	Ph	N-AA	OH	F	G1	H	HHH	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HHD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	DDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HHH	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HHD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	HDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	H	DDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HHH	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HHD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	DDD	H	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HHH	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HHD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	HDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	F	G1	D	DDD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HHH	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HHD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HDD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	DDD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HHH	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HHD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HDD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	DDD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HHH	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HHD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HDD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	DDD	H	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HHH	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HHD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	HDD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	D	DDD	D	—	—	H	—	—
PA	Ph	N-AA	F	OH	G1	H	HHH	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HHD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HDD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	DDD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HHH	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HHD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	HDD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	H	DDD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HHH	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HHD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HDD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	DDD	H	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HHH	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HHD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	HDD	D	—	—	D	—	—
PA	Ph	N-AA	F	OH	G1	D	DDD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HHH	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HHD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HDD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	DDD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HHH	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HHD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HDD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	DDD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HHH	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HHD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HDD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	DDD	H	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HHH	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HHD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	HDD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	D	DDD	D	—	—	H	—	—
PA	Ph	N-AA	F	F	G1	H	HHH	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HHD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HDD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	DDD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HHH	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HHD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	HDD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	H	DDD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HHH	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HHD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HDD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	DDD	H	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HHH	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HHD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	HDD	D	—	—	D	—	—
PA	Ph	N-AA	F	F	G1	D	DDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHH	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	DDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHH	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	DDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHH	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	DDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHH	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	HDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	D	DDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHH	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	DDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHH	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HHD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	HDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	H	DDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHH	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	DDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHH	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HHD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	HDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	OH	G1	D	DDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HHH	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HHD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	DDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HHH	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HHD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	DDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HHH	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HHD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	DDD	H	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HHH	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HHD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	HDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	D	DDD	D	—	—	H	—	—
PA	Naph	N-AA	OH	F	G1	H	HHH	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HHD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	DDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HHH	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HHD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	HDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	H	DDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HHH	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HHD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	DDD	H	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HHH	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HHD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	HDD	D	—	—	D	—	—
PA	Naph	N-AA	OH	F	G1	D	DDD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HHH	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HHD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HDD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	DDD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HHH	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HHD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HDD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	DDD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HHH	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HHD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HDD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	DDD	H	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HHH	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HHD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	HDD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	D	DDD	D	—	—	H	—	—
PA	Naph	N-AA	F	OH	G1	H	HHH	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HHD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HDD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	DDD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HHH	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HHD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	HDD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	H	DDD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HHH	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HHD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HDD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	DDD	H	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HHH	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HHD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	HDD	D	—	—	D	—	—
PA	Naph	N-AA	F	OH	G1	D	DDD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HHH	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HHD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HDD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	DDD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HHH	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HHD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HDD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	DDD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HHH	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HHD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HDD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	DDD	H	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HHH	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HHD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	HDD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	D	DDD	D	—	—	H	—	—
PA	Naph	N-AA	F	F	G1	H	HHH	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HHD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HDD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	DDD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HHH	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HHD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	HDD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	H	DDD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HHH	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HHD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HDD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	DDD	H	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HHH	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HHD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	HDD	D	—	—	D	—	—
PA	Naph	N-AA	F	F	G1	D	DDD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HHH	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HHD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HDD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	DDD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HHH	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HHD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HDD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	DDD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HHH	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HHD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HDD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	DDD	H	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HHH	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HHD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	HDD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	D	DDD	D	—	—	H	—	—
PA	POC	POC	OH	OH	G1	H	HHH	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HHD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HDD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	DDD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HHH	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HHD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	HDD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	H	DDD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HHH	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HHD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HDD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	DDD	H	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HHH	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HHD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	HDD	D	—	—	D	—	—
PA	POC	POC	OH	OH	G1	D	DDD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HHH	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HHD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HDD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	DDD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HHH	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HHD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HDD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	DDD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HHH	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HHD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HDD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	DDD	H	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HHH	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HHD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	HDD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	D	DDD	D	—	—	H	—	—
PA	POC	POC	OH	F	G1	H	HHH	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HHD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HDD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	DDD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HHH	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HHD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	HDD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	H	DDD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HHH	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HHD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HDD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	DDD	H	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HHH	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HHD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	HDD	D	—	—	D	—	—
PA	POC	POC	OH	F	G1	D	DDD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HHH	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HHD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HDD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	DDD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HHH	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HHD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HDD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	DDD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HHH	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HHD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HDD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	DDD	H	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HHH	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HHD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	HDD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	D	DDD	D	—	—	H	—	—
PA	POC	POC	F	OH	G1	H	HHH	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HHD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HDD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	DDD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HHH	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HHD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	HDD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	H	DDD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HHH	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HHD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HDD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	DDD	H	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HHH	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HHD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	HDD	D	—	—	D	—	—
PA	POC	POC	F	OH	G1	D	DDD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HHH	H	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HHD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HDD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	H	DDD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HHH	D	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HHD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HDD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	H	DDD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HHH	H	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HHD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HDD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	D	DDD	H	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HHH	D	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HHD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	D	HDD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	D	DDD	D	—	—	H	—	—
PA	POC	POC	F	F	G1	H	HHH	H	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HHD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HDD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	H	DDD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HHH	D	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HHD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	H	HDD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	H	DDD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HHH	H	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HHD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HDD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	D	DDD	H	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HHH	D	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HHD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	D	HDD	D	—	—	D	—	—
PA	POC	POC	F	F	G1	D	DDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHH	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	DDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHH	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	DDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHH	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	DDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHH	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	HDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	D	DDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHH	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	DDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHH	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HHD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	HDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	H	DDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHH	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	DDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHH	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HHD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	HDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	OH	G1	D	DDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HHH	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HHD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	DDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HHH	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HHD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	DDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HHH	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HHD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	DDD	H	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HHH	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HHD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	HDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	D	DDD	D	—	—	H	—	—
PA	P1	OH/O−	OH	F	G1	H	HHH	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HHD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	DDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HHH	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HHD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	HDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	H	DDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HHH	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HHD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	DDD	H	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HHH	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HHD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	HDD	D	—	—	D	—	—
PA	P1	OH/O−	OH	F	G1	D	DDD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HHH	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HHD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HDD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	DDD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HHH	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HHD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HDD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	DDD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HHH	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HHD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HDD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	DDD	H	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HHH	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HHD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	HDD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	D	DDD	D	—	—	H	—	—
PA	P1	OH/O−	F	OH	G1	H	HHH	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HHD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HDD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	DDD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HHH	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HHD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	HDD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	H	DDD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HHH	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HHD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HDD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	DDD	H	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HHH	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HHD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	HDD	D	—	—	D	—	—
PA	P1	OH/O−	F	OH	G1	D	DDD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HHH	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HHD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HDD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	DDD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HHH	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HHD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HDD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	DDD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HHH	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HHD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HDD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	DDD	H	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HHH	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HHD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	HDD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	D	DDD	D	—	—	H	—	—
PA	P1	OH/O−	F	F	G1	H	HHH	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HHD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HDD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	DDD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HHH	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HHD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	HDD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	H	DDD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HHH	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HHD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HDD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	DDD	H	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HHH	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HHD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	HDD	D	—	—	D	—	—
PA	P1	OH/O−	F	F	G1	D	DDD	D	—	—	D	—	—
PA	Ph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	D	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	OH	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	OH	F	G2	H	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	H	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	OH	F	G2	D	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HHH	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HHD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	DDD	H	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HHH	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HHD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	HDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	D	DDD	D	—	—	—	H	NH2
PA	Ph	N-AA	F	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Ph	N-AA	F	F	G2	H	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	H	DDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HHH	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HHD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	DDD	H	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HHH	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HHD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	HDD	D	—	—	—	D	NH2
PA	Ph	N-AA	F	F	G2	D	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	D	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	OH	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	OH	F	G2	H	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	H	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	OH	F	G2	D	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HHH	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HHD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	DDD	H	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HHH	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HHD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	HDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	D	DDD	D	—	—	—	H	NH2
PA	Naph	N-AA	F	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	Naph	N-AA	F	F	G2	H	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	H	DDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HHH	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HHD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	DDD	H	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HHH	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HHD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	HDD	D	—	—	—	D	NH2
PA	Naph	N-AA	F	F	G2	D	DDD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	POC	POC	OH	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	POC	POC	OH	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHH	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HHD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HDD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	DDD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HHH	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HHD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HDD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	DDD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HHH	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HHD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HDD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	DDD	H	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HHH	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HHD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	HDD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	D	DDD	D	—	—	—	H	NH2
PA	POC	POC	OH	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	OH	F	G2	H	HHH	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HHD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HDD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	DDD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HHH	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HHD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	HDD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	H	DDD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HHH	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HHD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HDD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	DDD	H	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HHH	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HHD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	HDD	D	—	—	—	D	NH2
PA	POC	POC	OH	F	G2	D	DDD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	POC	POC	F	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	POC	POC	F	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	POC	POC	F	F	G2	H	HHH	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HHD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HDD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	DDD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HHH	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HHD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HDD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	DDD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HHH	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HHD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HDD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	DDD	H	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HHH	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HHD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	HDD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	D	DDD	D	—	—	—	H	NH2
PA	POC	POC	F	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	POC	POC	F	F	G2	H	HHH	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HHD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HDD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	DDD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HHH	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HHD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	HDD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	H	DDD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HHH	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HHD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HDD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	DDD	H	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HHH	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HHD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	HDD	D	—	—	—	D	NH2
PA	POC	POC	F	F	G2	D	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	D	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	OH	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	OH	F	G2	H	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	H	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	OH	F	G2	D	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	D	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	OH	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	OH	G2	H	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	H	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	OH	G2	D	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHH	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	DDD	H	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHH	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	DDD	D	—	—	—	H	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HHH	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HHD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	DDD	H	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HHH	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HHD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	HDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	D	DDD	D	—	—	—	H	NH2
PA	P1	OH/O−	F	F	G2	H	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHH	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	DDD	H	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHH	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HHD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	HDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	D	DDD	D	—	—	—	D	OCH2CH3
PA	P1	OH/O−	F	F	G2	H	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	H	DDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HHH	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HHD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	DDD	H	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HHH	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HHD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	HDD	D	—	—	—	D	NH2
PA	P1	OH/O−	F	F	G2	D	DDD	D	—	—	—	D	NH2

P^A: -------- is absent and R^P is