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

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3789 C26H32N4O3 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-208 C1N(C)C(=O)CC1C(=O)N(c2ccccc2)CCCN3CCN(CC3)C(=O)c4ccccc4 4-(bromophenoxy)-1'-(2,6-dimethylbenzyl)-4'-methyl- 3790 C26H33BrN2O2 1,4'-bipiperidine c1cc(Br)ccc1OC2CCN(CC2)C3(C)CCN(CC3)C(=O)c4c(C)cccc4C 3791 C26H33BrN4O2 4-[(Z)-(4-bromophenyl)(ethoxyimino)]methyl]-1'-[(3- pyridinyl)carbonyl]-4'-methyl-1,4'-bipiperidine c1cc(Br)ccc1/C(=N\OCC)C2CCN(CC2)C3(C)CCN(CC3)C(=O)c4cccnc4 3792 C26H33BrN4O3 3793 C26H33ClN4O4 4-[(Z)-(4-bromophenyl)(ethoxyimino)]methyl]-1'-[(3- pyridinyl)carbonyl]-4'-methyl-1,4'-bipiperidine N-oxide 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4442-028 c1cc(Br)ccc1/C(=N\OCC)C2CCN(CC2)C3(C)CCN(CC3)C(=O)c4ccc[n+]([O-])c4 Nc1ccccc1C(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[C@@H](Cl)C[C@H]3C(=O)N C(C)(C)C 3794 C26H33N3O2 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-203 C1N(C)C(=O)CC1C(=O)N(c2ccccc2)CCCN3CCC(CC3)c4ccccc4 3795 C26H33N3O2 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-413 C1NC(=O)CC1C(=O)N(c2ccccc2)CCCN3CCC(CC3)Cc4ccccc4 3796 C26H33N3O3 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-212 C1N(C)C(=O)CC1C(=O)N(c2ccccc2)CCCN3CCC(CC3)Oc4ccccc4 3797 C26H34N2O4S HIV protease inhibitor; T-4049-005 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc4cncnc4 3798 C26H34N2O4S 4-hydroxy-5,6-dihydropyrone deriv., T-4013-005 CC(C)C1(CCc3cncnc3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3799 C26H34N2O5 HIV-1 protease inhibitor; T-4842-011 CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CCC(=O)N[C@@H]2[C@H](O)[C@]([ H])c3ccccc23 3800 C26H34N2OS 2-(alkylthio)-pyrimidin-4-ol deriv.; T-4130-109 CCCCCCCCCCCSc1nc(O)cc(n1)Cc2cccc3ccccc23 3801 C26H34N4O2 5-oxopyrrolidine-3-carboxamide deriv.; T-4823-207 C1N(C)C(=O)CC1C(=O)N(c2ccccc2)CCCN3CCN(CC3)Cc4ccccc4 3802 C26H34N4O8S3 4,4'-di[[(3-methio-1- carboxyl)propyl]aminomethylcarbonylamino] diphenylsulfone; NSC 40337 c1cc(NC(=O)CNC(C(=O)O)CCSC)ccc1S(=O)(=O)c2ccc(NC(=O)CNC(C(=O)O)CCSC)cc2 3803 C26H34N6O3S piperidine deriv.; T-4694-014 c1cc(NS(=O)(=O)C)cc2cc(nc12)C(=O)N3CCC(CC3)N(C5CC5)c4ncccc4NC(C)C 3804 C26H34O14 torachrysone gentiobioside Oc1c(C(=O)C)c(C)cc2cc(OC)cc(c12)O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@H](O3)C O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4 3805 C26H34O14 hirtellin A unavailable 3806 C26H34O4S2 HIV protease inhibitor (S); T-4049-111 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)C[C@@](OC2=O)(C(C)C)CCc3ccsc3 3807 C26H34O4S2 HIV protease inhibitor; T-4049-112 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)C[C@@](OC2=O)(C(C)C)CCc3ccsc3 3808 C26H34O4S2 HIV protease inhibitor; T-4049-010 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3cccs3 3809 C26H34O5S HIV protease inhibitor; T-4049-008 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3ccco3 3810 C26H34O5S HIV protease inhibitor; T-4049-009 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3ccoc3 3811 C26H34O5S 4-hydroxy-5,6-dihydropyrone deriv., T-4013-008 CC(C)C1(CCc3ccco3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2
3812 C26H34O5S 4-hydroxy-5,6-dihydropyrone deriv., T-4013-009 CC(C)C1(CCc3ccoc3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3813 C26H34O8 phorbol deriv.; T-4227-233 O=C1C(C)=C[C@@]2([H])[C@@]3(O)[C@H](C)[C@@H](OC(=O)C)[C@@](OC(=O)C)(C4( C)C)[C@]4([H])[C@]3([H])C=C(COC(=O)C)C[C@@]12[H] 3814 C26H34O8 RD3-2118; ingenol 3,5,20-triacetate; ITA O=C2[C@@]13/C=C(/C)[C@]([H])(O)[C@@]1(OC(=O)C)[C@]([H])(OC(=O)C)C(=C[C@@]2 ([H])[C@@]4([H])[C@@]([H])(C[C@]3(C)[H])C4(C)C)COC(=O)C 30220-45-2 3815 C26H34O9 phorbol deriv.; T-4227-143 O=C1C(C)=C[C@@]2([H])[C@@]3(O)[C@H](C)[C@@H](OC(=O)C)[C@@](OC(=O)C)(C4( C)C)[C@]4([H])[C@]3([H])C=C(COC(=O)C)C[C@@]12O 3816 C26H34O9 phorbol deriv.; T-4227-094 O=C1C(C)=C[C@@]2([H])[C@@]3(O)[C@H](C)[C@@H](OC(=O)C)[C@@](OC(=O)C)(C4( C)C)[C@]4([H])[C@]3([H])C=C(COC(=O)C)C[C@]12O 3817 C26H34O9 phorbol deriv.; T-4227-220 O=C1C5(C)C6[C@]2([H])[C@@]3(O)[C@H](C)[C@@H](OC(=O)C)[C@@](OC(=O)C)(C4(C )C)[C@]4([H])[C@]3([H])C6C5(COC(=O)C)C[C@@]12O 3818 C26H35ClN6O3S piperidine deriv.; T-4694-034 c1cc(NS(=O)(=O)C)cc2cc(nc12)C(=O)N3CCC(CC3)N(CC)c4nc(Cl)ccc4NC(C)(C)C 3819 C26H35FN6O3S piperidine deriv.; T-4694-035 c1cc(NS(=O)(=O)C)cc2cc(nc12)C(=O)N3CCC(CC3)N(CC)c4nc(F)ccc4NC(C)(C)C 3820 C26H35NO4S2 HIV protease inhibitor; T-4049-022 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3c(C)scn3 3821 C26H35NO4S2 HIV protease inhibitor; T-4049-021 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3csc(C)n3 3822 C26H35NO4S2 HIV protease inhibitor; T-4049-019 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3nc(C)cs3 3823 C26H35NO4S2 HIV protease inhibitor; T-4049-020 c1c(C)c(CO)cc(C(C)(C)C)c1SC2=C(O)CC(OC2=O)(C(C)C)CCc3ncc(C)s3 3824 C26H35NO4S2 4-hydroxy-5,6-dihydropyrone deriv., T-4013-022 CC(C)C1(CCc3c(C)scn3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3825 C26H35NO4S2 4-hydroxy-5,6-dihydropyrone deriv., T-4013-021 CC(C)C1(CCc3csc(C)n3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3826 C26H35NO4S2 4-hydroxy-5,6-dihydropyrone deriv., T-4013-019 CC(C)C1(CCc3nc(C)cs3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3827 C26H35NO4S2 4-hydroxy-5,6-dihydropyrone deriv., T-4013-020 CC(C)C1(CCc3ncc(C)s3)CC(O)=C(C(=O)O1)Sc2c(C(C)(C)C)cc(CO)c(C)c2 3828 C26H36BrN7O4S Trovirdine analogue; T-4171-102 n1cc(Br)ccc1NC(=S)NCCN2CCN(CC2)CCCCN3C(=O)C(C)=CN(C3=O)[C@H]4C=C[C@@ H](CO)o4 3829 C26H36BrN7O5S Trovirdine analogue; T-4171-104 n1cc(Br)ccc1NC(=S)NCCN2CCN(CC2)CCOCCN3C(=O)C(C)=CN(C3=O)[C@H]4C=C[C@ @H](CO)o4 3830 C26H36ClN3O7 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4442-013 CO[C@H]1OCC=C[C@@H]1OC(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[C@@H]( Cl)C[C@H]3C(=O)NC(C)(C)C 3831 C26H36ClN3O7 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4442-012 3-amino-2-hydroxy-4-phenylbutanoic acid deriv.; T- 4442-011 CO[C@H]1OCC=C[C@H]1OC(=O)N[C@@H](Cc2ccccc2)[C@H](O)C(=O)N3C[C@@H](Cl) C[C@H]3C(=O)NC(C)(C)C C1O[C@]2([H])[C@H](O)CO[C@]2([H])[C@@H]1OC(=O)N[C@@H](Cc2ccccc2)[C@H](O) C(=O)N3C[C@@H](Cl)C[C@H]3C(=O)NC(C)(C)C 3832 C26H36ClN3O8 OP(=O)([S- ])OC[C@H]2O[C@@H](n5cnc6c(OCCc7ccc(N(=O)=O)cc7)nc(N(CCCC)CCCC)nc56)[C@H]( 3833 C26H36N6NaO9PS B7 O)[C@@H]2O.[Na+] 3834 C26H36N6O3S piperidine deriv.; T-4694-019 c1cc(NS(=O)(=O)C(C)C)cc2cc(nc12)C(=O)N3CCC(CC3)N(CC)c4ncccc4NCC
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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-
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
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: 3767 C26H26O12 methyl 3,5-dicaffeoy
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 187 and 188: 4647 C35H38N2O3 cyclic urea deriv.;
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 195 and 196:
4798 C37H38N2O9 cyclic urea deriv.;
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 207 and 208:
Page 209 and 210:
5043 C42H52N6O8 L-mannaric acid dia
Page 211 and 212:
5075 C43H61N5O8 HIV protease inhibi
Page 213 and 214:
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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