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

2529 C18H14N2O3S2
1H-thieno[2,3-c][1,2,6]thiadiazin-4(3H)-one 2,2-dioxide
6-phenyl 3-benzyl
N1S(=O)(=O)N(Cc4ccccc4)C(=O)c2cc(sc12)c3ccccc3
2530 C18H14O6 NSC 518963 OC(=O)c1ccccc1C(=O)CCC(=O)c2ccccc2C(=O)O
2531 C18H14O8 2,3-di(3,4-dihydroxybenzylidene)succinic acid c1cc(O)c(O)cc1/C=C(C(=O)O)/C(C(=O)O)=C/c2cc(O)c(O)cc2
2532 C18H15ClN2O2S
2,2-dioxide-1,3-H-2,1,3-benzothiadiazine deriv.; T-
4836-008 c1cc(Cl)cc2C(C3CC3)(C#Cc4ccccc4)NS(=O)(=O)Nc12
2533 C18H15NO3S2
2-(benzamidoamido)-3-(4-
methylphenylsulfonyl)thiophene
c3ccccc3C(=O)Nc1sccc1S(=O)(=O)c2ccc(C)cc2
2534 C18H15N3O3S
2535 C18H15N3O3S2
2536 C18H16BrN3S
2537 C18H16BrN3S
1-[(phenylmethoxy)methyl]-1,5-dihydro-2H-pyrimido[4,5-
b][1,4]benzothiadine-2,4(3H)-dione
c4ccccc4COCN1C(=O)NC(=O)C2=C1Sc3ccccc3N2
1,1,3-trioxo-2H,4H-hetero[1,2,4]thiadiazine deriv.; T-
4696-023 c1scc2S(=O)(=O)N(Cc3ncccc3)C(=O)N(Cc4ccccc4)c12
N-[1-(1R)-(naphthyl)ethyl]-N'-[2-(5-
bromopyridyl)]thiourea
c1ccc2ccccc2c1C(C)NC(=S)Nc3ccc(Br)cn3
N-[1-(1S)-(naphthyl)ethyl]-N'-[2-(5-
bromopyridyl)]thiourea
c1ccc2ccccc2c1C(C)NC(=S)Nc3ccc(Br)cn3
2538 C18H16ClNO2S indolyl aryl sulfone deriv.; T-4561-035 c1cc(Cl)cc2c(Sc3cc(C)cc(C)c3)c(C(=O)OC)nc12
2539 C18H16ClNO2S indolyl aryl sulfone deriv.; T-4561-034 c1cc(Cl)cc2c(Sc3ccc(C)cc3C)c(C(=O)OC)nc12
2540 C18H16ClNO4S indolyl aryl sulfone deriv.; T-4561-049 c1cc(Cl)cc2c(S(=O)(=O)c3cc(C)cc(C)c3)c(C(=O)OC)nc12
2541 C18H16ClNO4S indolyl aryl sulfone deriv.; T-4561-048 c1cc(Cl)cc2c(S(=O)(=O)c3ccc(C)cc3C)c(C(=O)OC)nc12
2542 C18H16ClNO4S indolyl aryl sulfone deriv.; T-4561-014 c1cc(Cl)cc2n(c(C(=O)OCC)cc12)S(=O)(=O)c3ccc(C)cc3
2543 C18H16ClNO4S indolyl aryl sulfone deriv.; T-4561-019 c1cc(Cl)cc2n(cc(C(=O)OC(C)C)c12)S(=O)(=O)c3ccccc3
N-[1-(1R)-(naphthyl)ethyl]-N'-[2-(5-
chloropyridyl)]thiourea
c1ccc2ccccc2c1C(C)NC(=S)Nc3ccc(Cl)cn3
2544 C18H16ClN3S
2545 C18H16ClN3S
N-[1-(1S)-(naphthyl)ethyl]-N'-[2-(5-
chloropyridyl)]thiourea
c1ccc2ccccc2c1C(C)NC(=S)Nc3ccc(Cl)cn3
2546 C18H16N2O2S2 naphthalene derivative; T-4055-005 c1ncccc1C2SCCN2S(=O)(=O)c3cccc4ccccc34
2547 C18H16N2O3S benzothiadiazine dioxide deriv.; T-4194-016 C#CCCN2S(=O)(=O)N(Cc3ccccc3)C(=O)c4ccccc24
2548 C18H16N4O2 dipyridodiazepinone deriv.; T-4168-039 n1c(c4ccco4)ccc2N(C)C(=O)c3cccnc3N(c12)CC
2549 C18H16N4O2 dipyridodiazepinone deriv.; T-4168-040 n1c(c4ccoc4)ccc2N(C)C(=O)c3cccnc3N(c12)CC
2550 C18H16N4OS dipyridodiazepinone deriv.; T-4168-044 n1c(c4cccs4)ccc2N(C)C(=O)c3cccnc3N(c12)CC
2551 C18H16N4OS dipyridodiazepinone deriv.; T-4168-045 n1c(c4ccsc4)ccc2N(C)C(=O)c3cccnc3N(c12)CC
2552 C18H16N6O dipyridodiazepinone deriv.; T-4168-054 n1c(c4cnnc4)ccc2N(C)C(=O)c3cccnc3N(c12)C4CC4
2553 C18H16O3 HIV protease inhibitor; 4069-006 c1cccc2C(O)=C(C(=O)Oc12)C(CC)c3ccccc3
2554 C18H16O4 DZ-V-68 [C@@]12C=CC(OC)(CC1)C3=C2C(=O)c4cc(C)cc(O)c4C3=O
2555 C18H16O4 DZ-IV-137 c1ccc(O)c2C(=O)c3c(O)c(CC(C)C)ccc3C(=O)c12
2556 C18H16O6 alpha-conidendrol c1c(O)c(O)cc2C[C@@]3([H])C(=O)OC[C@]3([H])[C@H](c12)c4cc(O)c(O)cc4
2557 C18H16O6 beta-conidendrol c1c(O)c(O)cc2C[C@]3([H])C(=O)OC[C@]3([H])[C@H](c12)c4cc(O)c(O)cc4