Busqueda de Subestructura

Clc1cc2ccccc2cn1

Clc1cc2cccc(Cl)c2cn1
Reaction #68941
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc2ccccc2cn1
Reaction #68942
title compound
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CN(C)C)Oc1nc(Nc2cc3ccccc3cn2)cnc1C#N
Reaction #68943
title compound
Rendimiento 7.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc(Nc2cc3cccc(Cl)c3cn2)nc1O[C@@H]1CCNC1
Reaction #68944
(R)-5-(8-chloroisoquinolin-3-ylamino)-3-(pyrrolidin-3-yloxy)pyrazine-2-carbonitrile
Rendimiento 4.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1nc(Nc2cc3ccccc3cn2)cnc1C#N
Reaction #68968
ethyl 2-(3-cyano-6-(isoquinolin-3-ylamino)pyrazin-2-yloxy)acetate
Rendimiento 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1nc(Nc2cc3ccccc3cn2)cnc1C#N
Reaction #180834
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)NS(=O)(=O)C6CC6)CC5C=CCCCCN(C)C(=O)N4C3)ncc(Br)c2c1
Reaction #182930
DOI: 10.1039/C8SC04228D
Clc1cc2c(Br)cccc2c(Cl)n1
Reaction #183403
DOI: 10.1039/C8SC04228D
CC(C)(C)Oc1nc(Cl)cc2ccccc12
Reaction #184803
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc3ccccc3c(C3=C(c4c[nH]c5ccccc45)C(=O)NC3=O)n2)CC1
Reaction #187263
DOI: 10.1039/C8SC04228D
NC(=O)Cc1nc(Cl)cc2ccccc12
Reaction #197951
DOI: 10.1039/C8SC04228D
[O-][n+]1cc2ccccc2cc1Cl
Reaction #198199
DOI: 10.1039/C8SC04228D
Clc1cccc2c(N3CCSCC3)nc(N3CCNCC3)cc12
Reaction #202301
DOI: 10.1039/C8SC04228D
CCSc1cc2ccccc2c(=O)n1Cc1ccccc1
Reaction #202590
DOI: 10.1039/C8SC04228D
OCc1c(Cl)nc(-c2ccccc2)c2ccccc12
Reaction #207102
DOI: 10.1039/C8SC04228D
CN(C)Cc1c(Cl)nc(-c2ccccc2)c2ccccc12
Reaction #224236
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc3ccccc3cn2)CC1
Reaction #226429
DOI: 10.1039/C8SC04228D
Cc1cc(C)cc(P(c2cc(C)cc(C)c2)c2cc3ccccc3c(OC(C)(C)C)n2)c1
Reaction #238450
DOI: 10.1039/C8SC04228D
C=Cc1cc2cc(C(C)O)ccc2cn1
Reaction #245673
DOI: 10.1039/C8SC04228D
Cl
Reaction #246045
DOI: 10.1039/C8SC04228D
Página 1Siguiente