子结构搜索

118362

Nc1ncc(-c2ccncc2)c2scc(-c3ccc(NC(=O)Nc4cc(C(F)(F)F)ccc4F)cc3)c12
Reaction #45411
desired product
收率 46.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2n[nH]cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1)NCCO
Reaction #57144
N-(2-hydroxyethyl)-2-[3-(4-{[(phenylamino)carbonyl]amino}phenyl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)Cn2cc(-c3ccnc4[nH]ccc34)c(-c3ccc(NC(=O)Nc4ccccc4)cc3)n2)c1
Reaction #57145
title compound
收率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)Cn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57146
title compound
收率 13.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC(O)CO)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57149
title compound
收率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57209
title compound
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC3CCCO3)cc2Br)cc1
Reaction #57210
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc(-c2ccc(NC(=O)Nc3cc(C(F)(F)F)ccc3F)cc2)c1-c1cc2c(N)ncnc2s1
Reaction #60921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(c2ccc(C#N)c(C(F)(F)F)c2)C(=O)N1c1ccc(C(=O)O)c(F)c1
Reaction #67037
4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl)-2-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cc2c(N3CCOCC3)nc(-c3ccc(NC(=O)Nc4ccc(C(=O)N(C)C)cc4)cc3)nn2c1
Reaction #92072
solid
收率 25.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cc(N2C3CCC2COC3)nc(-c2ccc(NC(=O)Nc3ccc(N4CCN(C)CC4)cc3)cc2)n1
Reaction #162647
1-(4-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-((dimethylamino)methyl)pyrimidin-2-yl)phenyl)-3-(4-(4-methylpiperazin-1-yl)phenyl)urea
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2cc(C(=O)O)on2)cc1
Reaction #162957
title compound
收率 95.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)c1cc(-c2ccc(NC(=O)Nc3ccccc3)cc2)no1)C(=O)O
Reaction #162959
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc(NC(=O)NC3CCCCC3)cc2)no1
Reaction #162961
title compound
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)Nc1ccc(-c2cc(C(=O)O)on2)cc1
Reaction #162967
title compound
收率 95.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NC(=O)c1cc(-c2ccc(NC(=O)Nc3ccc(F)cc3)cc2)no1)C(C)C
Reaction #162968
title compound
收率 84.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)NC(=O)c1cc(-c2ccc(NC(=O)Nc3ccc(F)cc3)cc2)no1
Reaction #162970
title compound
收率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)Nc1ccc(-c2cc(C(=O)O)on2)cc1F
Reaction #162978
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCCN1C(=O)c1cc(-c2ccc(NC(=O)Nc3ccccc3F)cc2)no1
Reaction #163011
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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