子结构搜索

629478

CCOC(=O)c1cc2cc(NC(=O)C(CC)n3cc(OC)c(-c4cc(Cl)ccc4C#N)cc3=O)ccc2[nH]1
Reaction #85042
Ethyl 5-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoyl}amino)-1H-indole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)Nc1ccc2[nH]c(C(=O)O)cc2c1)n1cc(OC)c(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #85282
5-({2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoyl}amino)-1H-indole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(C(=O)Nc2ccc3[nH]c(C(=O)OC(C)(C)C)cc3c2)cc1
Reaction #180130
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(=O)CC(C)(C)C)ccc2n1Cc1ccccc1F
Reaction #195772
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(=O)CC(C)(C)C)ccc2n1Cc1ccccc1C(F)(F)F
Reaction #198537
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc2[nH]c(CO)cc2c1)C1(c2ccc3c(c2)OCO3)CC1
Reaction #221673
DOI: 10.1039/C8SC04228D
CC(C)(C)CC(=O)Nc1ccc2c(c1)cc(C(=O)O)n2Cc1ccccc1F
Reaction #300557
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(=O)c3ccc(OCC4CC4)cc3)ccc2[nH]1
Reaction #327077
title compound
收率 72.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(NC(=O)c3ccc(OCC4CC4)cc3)ccc2n1C
Reaction #327078
title compound
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C)c(NC(=O)c3ccc(OCC4CC4)cc3)ccc2n1C
Reaction #327086
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(NC(=O)c3ccccc3)ccc2n1C
Reaction #369428
DOI: 10.1039/C8SC04228D
CC(C)(C)CC(=O)Nc1ccc2c(c1)cc(C(=O)O)n2-c1ccccc1
Reaction #369656
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(=O)CC(C)(C)C)ccc2n1-c1ccccc1
Reaction #391257
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccc3[nH]c(C(=O)O)cc3c2)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F
Reaction #398859
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1cc2cc(NC(=O)c3cc4cc(CSSc5ccccn5)ccc4o3)ccc2[nH]1
Reaction #399757
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)ccc2[nH]1
Reaction #555604
ethyl 5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indole-2-carboxylate
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2[nH]c(CO)cc2c1)C1(c2ccc3c(c2)OCO3)CC1
Reaction #555631
1-(benzo[d][1,3]dioxol-5-yl)-N-(2-(hydroxymethyl)-1H-indol-5-yl)cyclopropanecarboxamide
收率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2cc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)ccc2[nH]1
Reaction #555632
5-(1-(benzo[d][1,3]-dioxol-5-yl)cyclopropanecarboxamido)-1H-indole-2-carboxylic acid
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2n1CC
Reaction #577171
title compound
收率 54.4%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(C(=O)O)cc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc21
Reaction #577172
1-Ethyl-5-[(4′-trifluoromethyl-biphenyl-2-carbonyl)-amino]-1H-indole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
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