Substructure Search

16875

O=C1Nc2c(ccc3c2CCNC3)C1=O
Reaction #5034
6,7,8,9-tetrahydro-1H-pyrrolo[2,3-f]isoquinoline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(N3CCc4c(N)cccc4C3)[nH]c(=O)c2cc1OC
Reaction #8826
2-(5-amino-3,4-dihydro-1H-isoquinolin-2-yl)-6,7-dimethoxy-3H-quinazolin-4-one
Yield 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc2c1CCN(C)C2
Reaction #76478
product
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCc2c(cccc2NC(C)=O)C1
Reaction #76479
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCc2c(cccc2NC(C)=O)C1
Reaction #76480
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(N)c([N+](=O)[O-])cc(Br)c2C1
Reaction #76481
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(N)c(N)cc(Br)c2C1
Reaction #76482
title compound
Yield 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(ccc(N)c2N)C1
Reaction #76483
title compound
Yield 48.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCc2c(ccc(N)c2N)C1
Reaction #76484
title compound
Yield 129.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(c(Br)cc3[nH]c(=O)c(=O)[nH]c23)C1
Reaction #76485
title compound
Yield 24.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #76503
9-Ethyl-1,4,7,8,9,10-hexahydro-6-nitro-pyrido[3,4-f]quinoxaline-2,3-dione
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1.CS(=O)(=O)O
Reaction #76504
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1.CS(=O)(=O)O
Reaction #76505
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc2[nH]c(=O)c(=O)[nH]c2c2c1CCN(C)C2
Reaction #76506
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(C#N)cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #76525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c(N4CCOCC4)nc(Cl)nc23)cc1
Reaction #81434
2-chloro-8-(4-methoxy-benzylamino)-4-morpholino-pyrimido[5,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(C(=O)Nc2cccc3c2CCNC3)Cc2ccccc2C1
Reaction #173265
DOI: 10.1039/C8SC04228D
CC(=O)N1CCc2c(cccc2NS(=O)(=O)c2ccccc2)C1
Reaction #175223
DOI: 10.1039/C8SC04228D
O=C(CC12CC3CC(CC(C3)C1)C2)Nc1cccc2c1CCN(Cc1ccc(F)cc1F)C2=O
Reaction #179128
DOI: 10.1039/C8SC04228D
COc1cc(N)c(Br)cc1C(=O)Nc1cccc2c1CCN(C)C2
Reaction #185878
DOI: 10.1039/C8SC04228D
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