Busqueda de Subestructura

Cc1cn(-c2ccc(N)cc2F)cn1

O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8244
title product
Rendimiento 66.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8245
desired product
Rendimiento 13.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc([N+](=O)[O-])cc2F)cn1
Reaction #8251
3-Fluoro-4-(4-methylimidazol-1-yl)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(N)cc2F)cn1
Reaction #8252
title compound
Rendimiento 90.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(NC(=O)OCc3ccccc3)cc2F)cn1
Reaction #8253
title product
Rendimiento 92.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(N3C[C@H](CO)OC3=O)cc2F)cn1
Reaction #8254
title product
Rendimiento 33.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(N3C[C@H](COS(C)(=O)=O)OC3=O)cc2F)cn1
Reaction #8255
title product
Rendimiento 78.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2N2CCSCC2)cn1)c1ccc(Cl)s1
Reaction #188763
DOI: 10.1039/C8SC04228D
O=C1CN(c2cc(-n3ccccc3=O)ccc2-n2cnc(CNC(=O)c3ccc(Cl)s3)c2)CCN1
Reaction #196561
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-n3cnc(COC(=O)c4ccco4)c3)c(F)c2)C(=O)O1
Reaction #398440
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-n3cnc(CN=[N+]=[N-])c3)c(F)c2)C(=O)O1
Reaction #406435
DOI: 10.1039/C8SC04228D
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2F)cn1)c1ccc(Cl)s1
Reaction #586955
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(-n2ccccc2=O)ccc1-n1cnc(CNC(=O)c2ccc(Cl)s2)c1
Reaction #586959
5-chloro-N-((1-(2-(methylthio)-4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2N2CCSCC2)cn1)c1ccc(Cl)s1
Reaction #586960
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(c2cc(-n3ccccc3=O)ccc2-n2cnc(CNC(=O)c3ccc(Cl)s3)c2)CCN1
Reaction #586961
title compound
Rendimiento 17.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2NCCO)cn1)c1ccc(Cl)s1
Reaction #586962
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2O)cn1)c1ccc(Cl)s1
Reaction #586963
title compound
Rendimiento 6.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2F)cn1)c1ccc(Cl)s1
Reaction #646715
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(-n2ccccc2=O)ccc1-n1cnc(CNC(=O)c2ccc(Cl)s2)c1
Reaction #646719
5-chloro-N-((1-(2-(methylthio)-4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cn(-c2ccc(-n3ccccc3=O)cc2N2CCSCC2)cn1)c1ccc(Cl)s1
Reaction #646720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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