Busqueda de Subestructura

1226874

NC1C2CC3CC1CC(Oc1cc4ccnc(OCc5ccccc5)c4cc1Cl)(C3)C2
Reaction #66732
title compound
Rendimiento 31.2%DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(Oc1cc4cc[nH]c(=O)c4cc1Cl)(C3)C2
Reaction #277329
DOI: 10.1039/C8SC04228D
N[C@H]1CC[C@@H](Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #489704
title compound
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN[C@H]1CC[C@@H](Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #489706
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN[C@H]1CC[C@@H](Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #489707
[4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-cis-cyclohexylamino]-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(Oc1cc4ccnc(OCc5ccccc5)c4cc1Cl)(C3)C2
Reaction #1240691
DOI: 10.1039/C8SC04228D
N[C@H]1CC[C@@H](Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #2000295
title compound
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3c(=O)[nH]ccc3c2Cl)CC1
Reaction #2000296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3c(=O)[nH]ccc3c2)CC1
Reaction #2000303
cis-6-(4-Amino-cyclohexyloxy)-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(N)CCC(Oc2cc3ccn(Cc4ccc(OC)cc4)c(=O)c3cc2Cl)CC1
Reaction #2457454
title compound ( 17 )
Rendimiento 25.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(N)CCC(Oc2ccc3c(=O)n(Cc4ccc(OC)cc4)ccc3c2)CC1
Reaction #2457455
6-(4-allyl-4-amino-cyclohexyloxy)-2-(4-methoxy-benzyl)-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CCCO)CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #2457463
title compound 53
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CC(O)CO)CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #2457464
[4-(1-benzyloxy-7-chloro-isoquinolin-6-yloxy)-1-(2,3-dihydroxy-propyl)-cyclohexyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CCCO)CCCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CCC1
Reaction #2457465
[5-(1-benzyloxy-7-chloro-isoquinolin-6-yloxy)-1-(3-hydroxy-propyl)-cyclooctyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CC(O)CO)CCCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CCC1
Reaction #2457468
[5-(1-benzyloxy-7-chloro-isoquinolin-6-yloxy)-1-(2,3-dihydroxy-propyl)-cyclooctyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccccc2)CCC(Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #2457472
title compound 71
Rendimiento 3.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](Oc2cc3ccncc3cc2Cl)CC1
Reaction #2457907
trans-[4-(7-Chloro-isoquinolin-6-yloxy)-cyclohexyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](Oc2cc3ccncc3cc2Cl)CC1
Reaction #2457908
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@@H](Oc2cc3ccncc3cc2Cl)CC1
Reaction #2457922
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2cc3cc[nH]c(=O)c3cc2Cl)CC1
Reaction #2489755
title compound
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente