部分構造検索

560293

CC(C)N1CCN(C(=O)c2ccc(NCCN3CCCCC3)nc2)CC1
Reaction #58743
title compound
収率 37.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C(c1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)nc1)N1CCN(CCO)CC1
Reaction #67771
1-(Benzo[d][1,3]dioxol-5-yl)-N-(5-((4-(2-hydroxyethyl)piperazin-1-yl)(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C(c1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)nc1)N1CCN(CCO)CC1
Reaction #67772
1-(Benzo[d][1,3]dioxol-5-yl)-N-(5-((4-(2-hydroxyethyl)piperazin-1-yl)(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(N)nc2)CC1.Cl
Reaction #71343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)OC(C)(C)C)nc2)CC1
Reaction #71344
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(F)c(OC)cc(OC)c4F)c4nccnc34)nc2)CC1
Reaction #71398
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4cc(OC)cc(OC)c4F)c4nccnc34)nc2)CC1
Reaction #71403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4cc(C)cc(OC)c4C)c4nccnc34)nc2)CC1
Reaction #71405
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(C)c(OC)cc(C)c4Cl)c4nccnc34)nc2)CC1
Reaction #71406
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(CCO)CC4)cn3)c3nccnc23)c1Cl
Reaction #71412
title compound
収率 76.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(N)nc3)C(C)(C)C2)cc1
Reaction #71419
title compound
収率 102.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(NC(=O)OC(C)(C)C)nc3)C(C)(C)C2)cc1
Reaction #71420
title compound
収率 35.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4cc(OC)cc(OC)c4)c4nccnc34)nc2)CC1
Reaction #71432
title compound
収率 35.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)cc(-c2ccc(C(=O)O)c3nccnc23)c1
Reaction #71434
title compound
収率 53.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(F)c(OC)cc(OC)c4Cl)c4nccnc34)nc2)CC1
Reaction #71458
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)nc2)CC1
Reaction #71477
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(NC(=O)c4ccc(-c5c(Cl)c(OC)cc(OC)c5Cl)c5cccnc45)nc3)CC2)cc1
Reaction #71478
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCNCC4)cn3)c3ncccc23)c1Cl
Reaction #71479
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2[nH]c(=O)c3cnn(C4CCOCC4)c3c2cc1C(=O)N1CCN(Cc2ccc(N3CCCC3)nc2)CC1
Reaction #156317
7-methyl-8-[(4-{[6-(pyrrolidin-1-yl)pyridin-3-yl]methyl}piperazin-1-yl)carbonyl]-1-(tetrahydro-2H-pyran-4-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCN(Cc2ccc(Nc3ncc4c5ccncc5n(C5CCCC5)c4n3)nc2)CC1
Reaction #166389
Compound 347
DOI: 10.6084/m9.figshare.5104873.v1
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