Substructure Search

19613

O=C(O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6975
4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6976
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6980
title compound
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(F)c(C=NOCc2ccccc2)c1F
Reaction #10374
title compound
Yield 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc(F)c(F)cc1Cl
Reaction #48876
title compound
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(F)cc1Cl
Reaction #52992
2,6-dichloro-4-fluorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C(=O)OC(C#N)c1ccc(F)c(Oc2ccccc2)c1)c1cc2ccccc2s1
Reaction #56210
α-cyano-4-fluoro-3-phenoxybenzyl 2-(2-benzothienyl)-3-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCN([C@H](C)[C@@](Cn2cncn2)(OS(=O)(=O)c2ccc(C)cc2)c2ccc(F)cc2F)CC1
Reaction #81940
(2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidine-1-yl)-1-(1H-1,2,4-triazole-1-yl)butane-2-ol p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCN([C@H](C)[C@](O)(Cn2cncn2)c2ccc(F)cc2F)CC1
Reaction #81941
(2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidine-1-yl)-1-(1H-1,2,4-triazole-1-yl)butane-2-ol
Yield 74.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cnc1N1CC(O)(c2ccc(F)cc2)C1
Reaction #159624
title compound
Yield 60.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(O)(c4ccc(F)cc4)C3)CC2)cc1
Reaction #159688
title compound ( D162 )
Yield 78.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(F)cc1Cl
Reaction #175270
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(F)c(F)c1Cl
Reaction #175922
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(CC(=O)c2ccc(F)cc2)cc1
Reaction #179062
DOI: 10.1039/C8SC04228D
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #183249
DOI: 10.1039/C8SC04228D
N#CC1CC1C(O)c1ccc(F)cc1Cl
Reaction #183459
DOI: 10.1039/C8SC04228D
Cc1c(I)c(OCc2ccc(F)cc2F)c(Br)c(=O)n1-c1c(F)cccc1F
Reaction #193583
DOI: 10.1039/C8SC04228D
CC(=O)OCc1c(-c2cc(Nc3ccc(N4CCOCC4)cn3)c(=O)n(C)c2)cc(F)cc1N1CCn2c(cc3c2CCCC3)C1=O
Reaction #195021
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCCc1ccsc1C(O)c1ccc(F)cc1
Reaction #197628
DOI: 10.1039/C8SC04228D
CCN1CC(c2ccc(Nc3cc(-c4cc(F)cc(N5CCn6c(cc7c6CCCC7)C5=O)c4COC(C)=O)cn(C)c3=O)nc2)C1
Reaction #198116
DOI: 10.1039/C8SC04228D
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