TerraTox - HIV-1 structure file, May 2004. Copyright ... - TerraBase Inc.

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4234 C31H34O16 4235 C31H34O16 crassirhizomoside B; kaempferol 3-alpha-L-(3,4-di-Oacetyl)rhamnopyranoside-7-alpha-L-rhamnopyranoside O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1Oc2cc3OC(c4ccc(O)cc4)=C(O[C@H] 5[C@H](O)[C@H](OC(=O)C)[C@@H](OC(=O)C)[C@H](C)O5)C(=O)c3c(O)c2 crassirhizomoside A; kaempferol 3-alpha-L-(2,4-di-Oacetyl)rhamnopyranoside-7-alpha-L-rhamnopyranoside O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1Oc2cc3OC(c4ccc(O)cc4)=C(O[C@H] 5[C@H](OC(=O)C)[C@H](O)[C@@H](OC(=O)C)[C@H](C)O5)C(=O)c3c(O)c2 4236 C31H34O16 crassirhizomoside C; kaempferol 3-alpha-L-(2,3-di-Oacetyl)rhamnopyranoside-7-alpha-L-rhamnopyranoside 5[C@H](OC(=O)C)[C@H](OC(=O)C)[C@@H](O)[C@H](C)O5)C(=O)c3c(O)c2 O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1Oc2cc3OC(c4ccc(O)cc4)=C(O[C@H] Cc1c(O)cc(F)cc1C(=O)N[C@@H](Cc2cc3ccccc3cc2)[C@H](O)C(=O)N3C[C@@H](Cl)C[C @H]3C(=O)NC(C)(C)C 4237 C31H35ClFN3O5 2-methyl-3-hydroxybenzamide deriv.; T-4443-050 4238 C31H35IN2O TAK-779 derivative; T-4053-005 c1cc(C)ccc1c2ccc3CCC(=Cc3c2)C(=O)Nc4ccc(cc4)C[N+]5(C)CCCCC5.[I-] 4239 C31H35IN2O TAK-779 derivative; T-4053-003 c1ccccc1c2ccc3CCC(=Cc3c2)C(=O)Nc4ccc(cc4)C[N+]5(C)CCCCCC5.[I-] 4240 C31H35IN2O TAK-779 derivative; T-4053-004 c1ccccc1c2ccc3CCC(=Cc3c2)C(=O)Nc4ccc(cc4)CC[N+]5(C)CCCCC5.[I-] 4241 C31H35IN2O2 TAK-779 derivative; T-4053-007 c1cc(C)ccc1c2ccc3OCCC(=Cc3c2)C(=O)Nc4ccc(cc4)C[N+]5(C)CCCCC5.[I-] Cc1c(O)cccc1C(=O)N[C@@H](Cc2c3ccccc3ccc2)[C@H](O)C(=O)N3C[C@@H](Cl)C[C@H ]3C(=O)NC(C)(C)C 4242 C31H36ClN3O5 2-methyl-3-hydroxybenzamide deriv.; T-4443-026 4243 C31H36ClN3O5 2-methyl-3-hydroxybenzamide deriv.; T-4443-027 4244 C31H36N2O8 hexanediamide deriv.; T-4449-184 4245 C31H36N4O3 cyclic urea deriv.; T-4423-043 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4246 C31H37ClN6O7 4441-043 Cc1c(O)cccc1C(=O)N[C@@H](Cc2ccc3ccccc3c2)[C@H](O)C(=O)N3C[C@@H](Cl)C[C@H ]3C(=O)NC(C)(C)C OCCNC(=O)[C@H](OCc1ccccc1)[C@H](O)[C@@H](O)[C@@H](OCc2ccccc2)C(=O)N[C@ @H]3[C@H](O)Cc4ccccc34 O[C@H]1[C@@H](Cc2ccccc2)N(Cc4cc(/C(=N/O)N)ccc4)C(=O)N(CC5CC5)[C@@H]1CCc3 ccccc3 n1oc2ccccc2c1C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3 C[C@@H](Cl)C[C@H]3C(=O)NC(C)(C)C 4247 C31H37N3O3 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-411 C1N(Cc5occc5)C(=O)CC1C(=O)N(c2ccccc2)CCCN3CCC(CC3)Cc4ccccc4 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- n1nc2ccccc2c1C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3 4248 C31H38ClN7O6 4441-042 C[C@@H](Cl)C[C@H]3C(=O)NC(C)(C)C 4249 C31H38N2O4 2-(tert-butoxycarbonylamino)-1,4-dibenzyl-2- hydroxypentanamide deriv.; T-4312-001 CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@](Cc2ccccc2)([H])C(=O)NCc3ccc cc3 4250 C31H38N2O4 L-364,505 deriv.; T-4328-014 CC(C)(C)OC(=O)N[C@H](Cc2ccccc2)[C@H](O)C[C@H](Cc2ccccc2)C(=O)NCc4ccccc4 4251 C31H38N2O7 cyclic urea deriv.; T-4415-025 O[C@H]1[C@@H](Cc2cc3OCCOc3cc2)N(CC4CC4)C(=O)N(CC4CC4)[C@H](Cc2cc3OCC Oc3cc2)[C@@H]1O 4252 C31H39F2N5O7 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-030 c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC (F)(F)C[C@H]3C(=O)NC(C)(C)C 4253 C31H39N3O9 AHPBA analogue; T-4457-050 c1ccccc1COC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N2CC C[C@H]2C(=O)OC(C)(C)C 4254 C31H39N5O7 1-[(3S)-3-(N2-benzyloxycarbonyl-L-asparginyl)amino-2- oxo-4-phenylbutyryl]-N-tert-butyl-L-prolinamide c3ccccc3COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)C(=O)N2CCC[C @H]2C(=O)NC(C)(C)C
4255 C31H39N5O7 4256 C31H39N5O8 1-[(3R)-3-(N2-benzyloxycarbonyl-L-asparginyl)amino-2- c3ccccc3COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@H](Cc1ccccc1)C(=O)C(=O)N2CCC[C@ oxo-4-phenylbutyryl]-N-tert-butyl-L-prolinamide H]2C(=O)NC(C)(C)C 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-033 c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC (=O)C[C@H]3C(=O)NC(C)(C)C 4257 C31H40BrN3O4 4258 C31H40BrN5O7 4259 C31H40ClN5O7 4260 C31H40ClN5O7 4261 C31H40ClN5O7 4262 C31H40FN5O7 4-[(Z)-(4-bromophenyl)(ethylacetatoimino)methyl]-1'- (2,6-dimethylbenzoyl)-4'-methyl-1,4'-bipiperidine 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-028 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-026 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-027 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-037 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4441-029 c1cc(Br)ccc1/C(=N\OCC(=O)OCC)C2CCN(CC2)C3(C)CCN(CC3)C(=O)c4c(C)cccc4C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@@H](Br)C[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@@H](Cl)C[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@H](Cl)C[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC [C@H](Cl)[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@@H](F)C[C@H]3C(=O)NC(C)(C)C 4263 C31H40N4O8 AHPBA analogue; T-4457-171; [Note: <strong>structure</strong> given identical to compound T-4349-131, but mp is different] c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N2CC C[C@H]2C(=O)OC(C)(C)C 4264 C31H40N4O8 tripeptide deriv.; T-4349-131; [Note: <strong>structure</strong> given identical to compound T-4457-171, but mp is different] 4265 C31H40N4O8 AHPBA analogue; T-4457-063 4266 C31H41N5O5S A-155704 4267 C31H41N5O7 tripeptide deriv.; T-4349-072 4268 C31H41N5O7 KNI-102 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4269 C31H41N5O8 4441-024 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4270 C31H41N5O8 4441-025 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4271 C31H41N5O8 4441-035 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4272 C31H41N5O8 4441-036 c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC C[C@H]3C(=O)OC(C)(C)C c1ccccc1OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N2CC C[C@H]2C(=O)OC(C)(C)C CN(C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc3ccccc3) NC(=O)OCc4scnc4 c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)C(=O)N3 CCC[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC C[C@H]3C(=O)NC(C)(C)C 139694-65-8 c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@@H](O)C[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[ C@H](O)C[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC [C@@H](O)[C@H]3C(=O)NC(C)(C)C c1ccccc1COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3CC [C@H](O)[C@H]3C(=O)NC(C)(C)C
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TerraTox - HIV-1 structure file, Ma
Page 3 and 4:
46 C8H9BrN2O5 47 C8H9BrN2O5 alpha-(
Page 5 and 6:
109 C8H11N3O3S (-)-2'-deoxy-3'-oxa-
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156 C9H9F2N3O3 157 C9H9F2N3O3 158 C
Page 9 and 10:
213 C9H10O4 214 C9H10O5 ethyl 3,4-d
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274 C9H13FN5O4P (2R/S)-6-amino-9-[2
Page 13 and 14:
325 C10H9F2N5O2 9-(2',3'-dideoxy-2'
Page 15 and 16:
376 C10H12FN5O2 2',3'-dideoxyadenos
Page 17 and 18:
433 C10H14FN3O3 1-(2-fluoro-2,3-did
Page 19 and 20:
484 C11H8ClNO2S2 thiazolothiazepine
Page 21 and 22:
545 C11H14N2O4 HEPT analogue; T-398
Page 23 and 24:
597 C12H8ClN5O2 5CITEP; 3-hydroxypr
Page 25 and 26:
645 C12H11ClFN3OS phenethylthiazoly
Page 27 and 28:
698 C12H14N2O3 pyridin-2-ol deriv.;
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749 C13H9BrN2OS 2-amino-6-arylsulfo
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794 C13H11ClN2O3S2 795 C13H11ClN2O3
Page 33 and 34:
843 C13H13ClN2O4S N-(3-chloro-6-ami
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898 C13H15N3OS2 N-(thiazol-2-yl)hio
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951 C14H7F6NO2 Efavirenz analogue;
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1003 C14H9N3S 2-amino-6-arylsulfony
Page 41 and 42:
1052 C14H11F4NO2 Efavirenz analogue
Page 43 and 44:
1096 C14H12N2O3S 2-amino-6-arylsulf
Page 45 and 46:
1142 C14H13N3O 5,11-dihydro-6H-pyri
Page 47 and 48:
1190 C14H15ClN2O2S 1191 C14H15ClN2O
Page 49 and 50:
1243 C14H16N2O3S HEPT derivative; T
Page 51 and 52:
1297 C14H17N3OS 2-(sec-butoxy)-4-am
Page 53 and 54:
1350 C15H8Cl2O3 3-hydroxyflavone, 3
Page 55 and 56:
1406 C15H11F3N2O2S 2-amino-6-arylsu
Page 57 and 58:
1459 C15H12O4 1,3-di(4-hydroxy-3-me
Page 59 and 60:
1510 C15H14FN3O 1511 C15H14FN3O 151
Page 61 and 62:
1558 C15H15N3O 5,11-dihydro-6H-pyri
Page 63 and 64:
1614 C15H16N4O dipyridodiazepinone
Page 65 and 66:
1673 C15H18N2O2S 2-(4-methylphenylt
Page 67 and 68:
1733 C15H19N3O2 pyrid-2-ol deriv.;
Page 69 and 70:
1786 C16H6O8S 3,4-dicarboxylic acid
Page 71 and 72:
1827 C16H13ClF3N3O 6,11-dihydro-5H-
Page 73 and 74:
1884 C16H15F3N2O3 Efavirenz analogu
Page 75 and 76:
1939 C16H16N2O4S NSC 667948 c1c([H]
Page 77 and 78:
1991 C16H18Cl2N2OS pyrimidin-4-ol d
Page 79 and 80:
2054 C16H19N3O3S pyrimidin-4-ol der
Page 81 and 82:
2117 C16H20N2O4 2118 C16H20N2O4S OC
Page 83 and 84:
2180 C16H24N6O5 2181 C16H26N2O5Si 2
Page 85 and 86:
2231 C17H15ClN2O4S indolyl aryl sul
Page 87 and 88:
2294 C17H17N2O7P 7-methyl-cyclo-sal
Page 89 and 90:
2350 C17H19ClF2N4S phenethylthiazol
Page 91 and 92:
2405 C17H20N2O3 N-benzyl-6,7-dihydr
Page 93 and 94:
2472 C17H23N3O TIBO deriv.; T-4175-
Page 95 and 96:
2529 C18H14N2O3S2 1H-thieno[2,3-c][
Page 97 and 98:
2587 C18H18N2O2 pyridin-2-ol deriv.
Page 99 and 100:
threo-2,3-di(3,4-dihydroxybenzyl)su
Page 101 and 102:
2702 C18H24ClN3S R86162 c1c(Cl)cc2N
Page 103 and 104:
2756 C18H31N3O8SSi 2757 C18H31N3O8S
Page 105 and 106:
2803 C19H18BrN5OS N-[2-(6,7-dihydro
Page 107 and 108:
2855 C19H20N5O5P 3-methyl-cyclo-sal
Page 109 and 110:
2908 C19H24O9 chromene glucuside Cc
Page 111 and 112:
2966 C20H17N2O7P benzo[c]-cyclo-sal
Page 113 and 114:
3026 C20H21N3O TIBO deriv.; T-4169-
Page 115 and 116: 3075 C20H24N4O2 6,11-dihydro-5H-pyr
Page 117 and 118: 3126 C21H14F4N2 1,2-diphenylbenzimi
Page 119 and 120: 3190 C21H20Br2O6 alkenyldiarylmetha
Page 121 and 122: 3248 C21H23N3O2 bis(heteroaryl)pipe
Page 123 and 124: 3291 C21H29ClN4O2 bis(heteroaryl)pi
Page 125 and 126: 3343 C22H20ClN5O2 diazepinone deriv
Page 127 and 128: 3402 C22H26O5 (+)-cathonolide A O[C
Page 129 and 130: 3446 C22H31NO5 3449 C22H33NO4 estra
Page 131 and 132: 3499 C23H22N2O6S2 1H-thieno[2,3-c][
Page 133 and 134: 3538 C23H28O5 10,11-cis-10,11-dihyd
Page 135 and 136: 3585 C24H24O12 1,4,8-trihydroxynaph
Page 137 and 138: 3630 C24H42IN3O8SSi2 TSAO deriv.; T
Page 139 and 140: 3674 C25H24O12 (-)-3,5-dicaffeoyl-m
Page 141 and 142: 3721 C25H34N10NaO9PS B1 C1[C@H](n3c
Page 143 and 144: 3767 C26H26O12 methyl 3,5-dicaffeoy
Page 145 and 146: 3812 C26H34O5S 4-hydroxy-5,6-dihydr
Page 147 and 148: 3859 C27H25N3O2 cyclic urea deriv.;
Page 149 and 150: 3900 C27H34BrN3O3 1'-(2-hydroxy-6-m
Page 151 and 152: 3939 C27H36N2O5S2 4-hydroxy-5,6-dih
Page 153 and 154: 3981 C28H31N5O2 1-[(6-benzyloxy-1H-
Page 155 and 156: 4017 C28H36ClN3O6 2-methyl-3-hydrox
Page 157 and 158: 4057 C28H40N8O3S piperidine deriv.;
Page 159 and 160: 4097 C29H37F3N4O4 4098 C29H37NO8 4-
Page 161 and 162: 4136 C29H50N4O11SSi2 4137 C29H51N5O
Page 163 and 164: 4175 C30H41N3O2 5-oxopyrrolidine-3-
Page 165: 4214 C31H20O6 3,3'-(4-phenylbezylid
Page 169 and 170: N-3-benzoyloxymethyl / N-3-carboxym
Page 171 and 172: 4332 C32H37IN2O TAK-779 derivative;
Page 173 and 174: 4374 C32H44O8 cucurbitacin E CC1(C)
Page 175 and 176: 4411 C33H22O8 3,3'-(4-stilbenomethy
Page 177 and 178: 4452 C33H37Cl2N3O2 5-oxopyrrolidine
Page 179 and 180: 4491 C33H40N2O7 N-(2(R)-hydroxy-1(S
Page 181 and 182: 4528 C33H53NO4 betulinic acid deriv
Page 183 and 184: 4569 C34H40ClN3O5 2-methyl-3-hydrox
Page 185 and 186: 4609 C34H51N5O8 hydroxyethylhydrazi
Page 189 and 190: 4685 C35H46O9 phorbol deriv.; T-422
Page 191 and 192: 4723 C36H38N2O6S cyclic sulfondiami
Page 193 and 194: 4761 C36H55NO6 triterpene acid / he
Page 197 and 198: 4837 C37H58O6 3-(3,3-dimethyl-1,5-p
Page 199 and 200: 4873 C38H47N5O7S tripeptide deriv.;
Page 201 and 202: 4909 C38H63NO4 betulinic acid deriv
Page 203 and 204: 4942 C39H53N7O7 hydroxyethylhydrazi
Page 205 and 206: 4977 C40H53N5O8 meta-/paracyclophan
Page 209 and 210: 5043 C42H52N6O8 L-mannaric acid dia
Page 211 and 212: 5075 C43H61N5O8 HIV protease inhibi
Page 215 and 216: 5138 C47H46N6O5 SB-570 5139 C47H46N
Page 217 and 218:
5168 C48H82N2O5 betulinic acid deri
Page 219 and 220:
5196 C55H81N5O14 Indinavir-PEG350(8
show all

TerraTox - HIV-1 structure file, May 2004. Copyright ... - TerraBase Inc.

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