Busqueda de Subestructura

CNc1ccccc1

Cn1c(Nc2ccc(Br)c(F)c2)nc2cc(OC3(C4CCNC(CCNC=O)C4)C=CC=CN3)ccc21
Reaction #41743
4-(2-{[4-bromo-3-fluorophenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-piperidylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(Nc2cccc(C(C)(C)C)c2)nc2cc(OC3(C4CCNC(CCNC=O)C4)C=CC=CN3)ccc21
Reaction #41748
4-(2-{[3-(tert-butyl)phenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-piperidylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(F)c2)c(CCCOc2cccc(F)c2)n1
Reaction #84532
title compound
Rendimiento 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1)c1ccccc1
Reaction #164764
title compound
Rendimiento 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)cn1
Reaction #164766
title compound
Rendimiento 92.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)nc1
Reaction #164770
title compound
Rendimiento 92.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)CC2CS1
Reaction #164773
title compound
Rendimiento 186.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164774
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1
Reaction #164775
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164776
title compound
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1.Cl
Reaction #164777
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)nc1
Reaction #164778
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cccc(NC(=O)c4ncc(F)cc4F)c3)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164779
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)nc1
Reaction #164780
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ncc(F)cc4F)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164781
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Nc1ccc(-c2nc(-c3ccc(NC(=O)Nc4cccc(C(N)=O)c4)cc3)nc(N3C(C)COCC3C)n2)cc1
Reaction #184870
DOI: 10.1039/C8SC04228D
COC(=O)C(C)(C)c1ccc(NC(=O)C(C2CCCCC2)n2c(-c3ccc(Cl)cc3)nc3cc(F)c(F)cc32)c(F)c1
Reaction #191791
DOI: 10.1039/C8SC04228D
CC1CN(c2cc3c(c(NCc4ccccc4)c2F)c(=O)c(C(=O)O)cn3C2CC2)CCN1
Reaction #196055
DOI: 10.1039/C8SC04228D
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4cccc(Cl)c4)c(C)c3)c2cc1OC
Reaction #202253
DOI: 10.1039/C8SC04228D
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