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

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4854 C37H61NO4 betulinic acid deriv.; T-4396-008 4855 C37H64N2O8Si3 N-3-benzoyloxymethyl / N-3-carboxymethyl pyrimid-2,4- dione deriv.; T-4254-007 4856 C38H38N2O4 cyclic urea deriv.; T-4100-071 4857 C38H38N2O7 cyclic urea deriv.; T-4429-014 4858 C38H38N4O5 cyclic urea deriv.; T-4570-121 4859 C38H39N5O4 SD-145 4860 C38H40F2N4O8 L-mannaric acid diamide deriv.; T-4515-042 4861 C38H40N2O4 4862 C38H40N2O7 GW-5950X; 2(R)-benzyl-5-[3(R),5(R)-dibenzyl-2- oxopyrrolidin-1-yl]-4(S)-hydroxy-N-[2(R)-hydroxyindan- 1(S)-yl]pentanamide N1,N6-di[2R-hydroxy-1S-indanyl)-2R,5R-dibenzyloxy- 3R-hydroxyhexandiamide 4863 C38H40N2O8 HIV-1 protease inhibitor; T-4067-038 4864 C38H40N2O8 HIV-1 protease inhibitor; T-4067-037 4865 C38H40N2O8 L-mannaric acid diamide deriv.; T-4515-044 N1,N6-di[2R-hydroxy-1S-indanyl)-2R,5R-dibenzyloxy- 4866 C38H40N2O8 3R,4R-dihydroxyhexandiamide 4867 C38H40O20 flavanoid glycoside; T-4228-007 4868 C38H42N4O10 HIV-1 protease inhibitor; T-4067-024 4869 C38H42N4O7 cyclic urea deriv.; T-4415-017 4870 C38H42N4O8 L-mannaric acid diamide deriv.; T-4515-041 4871 C38H45Cl2N5O7 kynostatin deriv.; T-4359-013 4872 C38H45N5O7 kynostatin deriv.; T-4359-012 C1(C)(C)[C@@H](O)CC[C@]2(C)[C@@]3([H])CC[C@]4([H])[C@@]5([H])[C@]([H])(C(C)=C )CC[C@]5(C(=O)N[C@H](C(=O)OC)CC(C)C)CC[C@@]4(C)[C@]3(C)CC[C@@]12([H]) [C@@H]1(O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO[Si](C)(C)C(C)(C) C)O[C@H]1N2C=C(C)C(=O)N(CC(=O)OCc3ccccc3)C2=O [C@@]1([H])(O)[C@@H](Cc2ccccc2)N(Cc4ccc5ccccc5c4)C(=O)N(Cc6ccc(CO)cc6)[C@H]( Cc3ccccc3)[C@@H]1O O[C@H]1[C@@H](Cc2ccccc2)N(Cc3cc(C(=O)OC)ccc3)C(=O)C(=O)N(Cc2cc(C(=O)OC)ccc 2)[C@@H]1CCc3ccccc3 c1ccccc1C[C@@]2([H])(N(Cc3cc(c6nncc6)ccc3)C(=O)N[C@H](Cc5ccccc5)[C@H](O)[C@]2 (O)[H] O[C@H]1[C@@H](Cc2ccccc2)N(CC5CC5)C(=O)N(Cc4cc(C(=O)Nc6nc7ccccc7n6)ccc4)[C @H](Cc3ccccc3)[C@@H]1O CNC(=O)[C@H](c3cc(F)ccc3)NC(=O)[C@H](OCc1ccccc1)[C@H](O)[C@@H](O)[C@@H]( OCc2ccccc2)C4(=O).CNC(=O)[C@H](c5cc(F)ccc5)N4 c1ccccc1C[C@H]2C[C@H](c3ccccc3)N(C2=O)C[C@@H](O)C[C@@H](Cc4ccccc4)C(=O)N [C@@H]5[C@H](O)Cc6ccccc56 O[C@@H]1Cc2ccccc2[C@@H]1NC(=O)[C@H](OCc1ccccc1)[C@H](O)C[C@@H](OCc2cc ccc2)C(=O)N[C@@H]3[C@H](O)Cc4ccccc34 c1ccccc1CO[C@@H](C(=O)N[C@@H]3c4ccccc4C[C@@H]3O)[C@H](O)[C@@H](O)[C@ @H](OCc2ccccc2)C(=O)N[C@@H]3c4ccccc4C[C@@H]3O c1ccccc1CO[C@@H](C(=O)N[C@H]3c4ccccc4C[C@H]3O)[C@H](O)[C@@H](O)[C@@H]( OCc2ccccc2)C(=O)N[C@H]3c4ccccc4C[C@H]3O c3cccc4C[C@H](O)[C@@H](c34)NC(=O)[C@H](OCc1ccccc1)[C@H](O)[C@@H](O)[C@@ H](OCc2ccccc2)C5(=O).c3cccc4C[C@H](O)[C@@H](c34)N5 O[C@@H]1Cc2ccccc2[C@@H]1NC(=O)[C@H](OCc1ccccc1)[C@H](O)[C@@H](O)[C@@ H](OCc2ccccc2)C(=O)N[C@@H]3[C@H](O)Cc4ccccc34 Oc1cc(O)cc2OC(c3cc(O)c(O)cc3)=C(C(=O)c12)[C@@H]1O[C@H](CO)[C@H](O)[C@H](O) [C@H]1O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@H](O2)COC(=O)/C=C/c3cc(OC)c(O)c (OC)c3 c1ccccc1CO[C@@H](C(=O)N[C@H](C(=O)NC)c3ccc(O)cc3)[C@H](O)[C@@H](O)[C@@H ](OCc2ccccc2)C(=O)N[C@H](C(=O)NC)c3ccc(O)cc3 O[C@H]1[C@@H](Cc2cc3OCCOc3cc2)N(Cc3cccc(N)c3)C(=O)N(Cc3cccc(NC)c3)[C@H](C c2cc3OCCOc3cc2)[C@@H]1O c1ccccc1CO[C@@H](C(=O)N[C@H](C(=O)NC)c3ccccc3)[C@H](O)[C@@H](O)[C@@H](O Cc2ccccc2)C(=O)N[C@H](C(=O)NC)c3ccccc3 c1cc(Cl)ccc1C(c2ccc(Cl)cc2)OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc3ccccc3)[C @H](O)C(=O)N4CCC[C@H]4C(=O)NC(C)(C)C c1cccc2c3ccccc3C(c12)COC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc3ccccc3)[C@H]( O)C(=O)N4CCC[C@H]4C(=O)NC(C)(C)C
4873 C38H47N5O7S tripeptide deriv.; T-4349-234 4874 C38H47N5O7S tripeptide deriv.; T-4349-235 4875 C38H47N5O7S tripeptide deriv.; T-4349-236 4876 C38H48N4O6S2 KNI-226 4877 C38H48N6O7S KNI-241 4878 C38H48N6O8S2 L-mannaric acid diamide deriv.; T-4514-011 4879 C38H49N3O6 pseudo peptide, T-4330-047 4880 C38H49N5O5 L-364,505 deriv.; T-4328-017 4881 C38H49N5O7 OE 4882 C38H50N2O10 4-aryl-1,4-dihydropyridine dimer; T-4199-016 4883 C38H50N2O7 pseudo peptide, T-4330-042 4884 C38H50N6O5 HIV-1 protease inhibitor; T-4842-041 4885 C38H51N3O5 pseudo peptide, T-4330-016 4886 C38H51N3O5 L-364,505 deriv.; T-4328-010 4887 C38H51N5O7 2-ethoxyhydrazine deriv.; T-4416-241 4888 C38H51N5O7 2-ethoxyhydrazine deriv.; T-4416-231 4889 C38H51N7O7 hydroxyethylhydrazine deriv.; T-4391-321 4890 C38H52N6O7 Atazanavir; BMS 232632 4891 C38H52N6O7 CGP 73547 4892 C38H52N6O8S Saquinavir mesylate; Invirase; Fortovase c1ccccc1c2c(cccc12)OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O) C(=O)N3CSC(C)(C)[C@H]3C(=O)NC(C)(C)C c1ccccc1c2cc(ccc12)OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O) C(=O)N3CSC(C)(C)[C@H]3C(=O)NC(C)(C)C c1ccccc1c2ccc(cc12)OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H](O) C(=O)N3CSC(C)(C)[C@H]3C(=O)NC(C)(C)C c1ccccc1c2cccc(c12)OCC(=O)N[C@@H](CSC)C(=O)N[C@@H](Cc3ccccc3)[C@H](O)C(= O)N4CSC(C)(C)[C@H]4C(=O)NC(C)(C)C c1ccccc1Nc2cc(ccc12)OCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc2ccccc2)[C@H]( O)C(=O)N3CSC(C)(C)[C@H]3C(=O)NC(C)(C)C CNC(=O)[C@H](C(C)C)NC(=O)[C@H](OCc1ccc(c5nccs5)cc1)[C@H](O)[C@@H](O)[C@@ H](OCc2ccc(c5nccs5)cc2)C4(=O).CNC(=O)[C@H](C(C)C)N4 CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@@H](Cc4ccc(CN5CCOCC5)cc4) C(=O)N[C@]2([H])[C@H](O)Cc3ccccc23 CC(C)(C)OC(=O)N[C@H](Cc2ccccc2)[C@H](O)C[C@H](Cc2ccccc2)C3(=O).CC[C@@H](C )[C@H](N3)C(=O)NCc4nc5ccccc5n4 c1ccccc1CC(NC(=O)OC(C)(C)C)CCNC(Cc2ccccc2)C(=O)NC(CCC(=O)O)C(=O)NC(Cc3ccc cc3)C(=O)N [C@]36(CO)[C@]2([H])[N@](C(=O)OC(C)(C)C)[C@]5([H])[C@]4(CO)[C@@]([H])(c1ccc(OC )cc1)[C@@]2(CO)[C@]3([H])[N@](C(=O)OC(C)(C)C)[C@]4([H])[C@]5(CO)[C@]6([H])c7ccc (OC)cc7 CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@@H](Cc4ccc(CCC(OC)OC)cc4) C(=O)N[C@]2([H])[C@H](O)Cc3ccccc23 c1cccc2ccc(nc12)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc3ccccc3)[C@H](O)CN4[C @H](C(=O)NC(C)(C)C)C[C@]5([H])CCCCC5([H])C4 CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@@H](Cc4ccc(CCCN(C)C)cc4)C( =O)N[C@]2([H])[C@H](O)Cc3ccccc23 CC(C)(C)OC(=O)N[C@H](Cc2ccccc2)[C@H](O)C[C@H](Cc2ccccc2)C4(=O).CC(C)C[C@H] (N4)C(=O)NCCc5ccccc5 c1ccccc1C[C@H](NC(=O)[C@H](C(C)(C)C)NC(=O)OC)[C@@H](O)CN(Cc2ccc(c3ccccc3)c c2)NC(=O)[C@H](C(C)C)NC(=O)OC c1ccccc1C[C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(Cc2ccc(c3ccccc3)cc2) NC(=O)[C@H](C(C)(C)C)NC(=O)OC c1cc2ccccc2nc1C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](Cc3ccccc3)[C@@H](O)CN(C C4CCCCC4)NC(=O)C(NC(=O)OC)C(C)C C(OC)(=O)N[C@@H](C(C)(C)C)C(=O)NN(Cc2ccc(c1ncccc1)cc2)C[C@H](O)C(Cc3ccccc3) NC(=O)[C@H](C(C)(C)C)NC(OC)=O 198904-31-3 c1ccccc1C[C@H](NC(=O)[C@H](C(C)(C)C)NC(=O)OC)[C@@H](O)CN(Cc2ccc(c3ccccn3)c c2)NC(=O)[C@H](C(C)(C)C)NC(=O)OC c1cccc2ccc(nc12)C(=O)N[C@@H](C(=O)N)C(=O)N[C@@H](Cc3ccccc3)[C@H](O)CN4C[C @@]5([H])CCCC[C@@]5([H])C[C@H]4C(=O)NC(C)(C)C.OS(=O)(=O)C 149845-06-7
Page 1 and 2:
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-
Page 7 and 8:
156 C9H9F2N3O3 157 C9H9F2N3O3 158 C
Page 9 and 10:
213 C9H10O4 214 C9H10O5 ethyl 3,4-d
Page 11 and 12:
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.;
Page 29 and 30:
749 C13H9BrN2OS 2-amino-6-arylsulfo
Page 31 and 32:
794 C13H11ClN2O3S2 795 C13H11ClN2O3
Page 33 and 34:
843 C13H13ClN2O4S N-(3-chloro-6-ami
Page 35 and 36:
898 C13H15N3OS2 N-(thiazol-2-yl)hio
Page 37 and 38:
951 C14H7F6NO2 Efavirenz analogue;
Page 39 and 40:
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
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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
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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 and 166: 4214 C31H20O6 3,3'-(4-phenylbezylid
Page 167 and 168: 4255 C31H39N5O7 4256 C31H39N5O8 1-[
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: 4837 C37H58O6 3-(3,3-dimethyl-1,5-p
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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