部分構造検索

556672

CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57130
title product
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)NC(C)C)cc2)n1
Reaction #57131
title product
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)N3CCOCC3)cc2)n1
Reaction #57132
title product
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)N3CCCC3)cc2)n1
Reaction #57133
title product
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Nc3cccc(-c4ccccc4)c3)cc2)n1
Reaction #57134
title product
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(N(C)C(=O)Nc3ccccc3)cc2)n1
Reaction #57135
title product
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1ccc(-c2nn(CC)cc2-c2c(F)cnc3[nH]ccc23)cc1
Reaction #57136
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2c(F)cnc3[nH]ccc23)c(-c2ccc(NC(=O)N(C)C)cc2)n1
Reaction #57137
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1ccc(-c2nn(CC)cc2-c2c(C)cnc3[nH]ccc23)cc1
Reaction #57138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2c(C)cnc3[nH]ccc23)c(-c2ccc(NC(=O)N(C)C)cc2)n1
Reaction #57139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(C4=CCNCC4)cc23)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57140
title compound
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)OC)cc2)n1
Reaction #57141
title product
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3ccnc4[nH]ccc34)c(-c3ccc(NC(=O)Nc4ccccc4)cc3)n2)cc1
Reaction #57142
title product
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
収率 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
収率 13.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC3CCCO3)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57147
title compound
収率 11.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC(F)(F)F)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57148
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC(O)CO)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57149
title compound
収率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(NC(=O)Cc3cccs3)cc2)n1
Reaction #57152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ