Busqueda de Subestructura

4530

Fc1cccc(F)c1-c1ccc2cccnc2n1
Reaction #926
desired product
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCC(=O)c1c(F)cccc1F
Reaction #53289
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)ccc1C(=O)c1c(F)cccc1F
Reaction #58426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(Nc2ccc(C(=O)c3c(F)cccc3F)c(N)n2)CC1
Reaction #58427
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(Nc2nc(N)c(C(=O)c3c(F)cccc3F)s2)CC1
Reaction #58440
[4-amino-2-(1-methanesulfonylpiperidin-4-ylamino)thiazol-5-yl]-(2,6-difluorophenyl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CNc1ccc(F)cc1F)C(=O)c1c(F)c(F)c(F)c(F)c1F
Reaction #64983
title compound
Rendimiento 94.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2ccc(F)cc2F)c2c(F)c(F)c(F)c(F)c2c1=O
Reaction #64984
title compound
Rendimiento 94.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCN(c1ccc(F)c(C(C)=O)c1F)S(=O)(=O)c1cc(F)ccc1F
Reaction #74174
N-(3-acetyl-2,4-difluoro-phenyl)-2,5-difluoro-N-(2-methoxy-ethoxymethyl)-benzene-sulfonamide
Rendimiento 62.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F.Cl
Reaction #88343
Vemurafenib HCl
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F.Cl
Reaction #88344
Vemurafenib HCl
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F.Cl
Reaction #88345
Vemurafenib HCl
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Br)cc23)c1F
Reaction #88360
desired compound
Rendimiento 100.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Br)cc23)c1F
Reaction #88361
desired compound
Rendimiento 103.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Br)cc23)c1F
Reaction #88362
desired compound
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2cn(C(=O)c3c(Cl)cccc3Cl)c3ncc(Br)cc23)c1F
Reaction #88363
desired compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc5[nH]ncc5c4)cc23)c1F
Reaction #88364
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2cn(C(=O)c3c(Cl)cccc3Cl)c3ncc(-c4ccc5[nH]ccc5c4)cc23)c1F
Reaction #88365
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc5c(cnn5C(C)=O)c4)cc23)c1F
Reaction #88366
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4cn[nH]c4)cc23)c1F
Reaction #88373
Propane-1-sulfonic acid {2,4-difluoro-3-[5-(1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-phenyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4cnn(C(=O)Oc5ccccc5)c4)cc23)c1F
Reaction #88374
desired compound
Rendimiento 6.2%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente