Busqueda de Subestructura

985573

c1ccc(C(OC2CN(CCCOCCc3ccc4sccc4c3)C2)(c2ccccc2)c2ccccc2)cc1
Reaction #7553
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-(trityloxy)azetidine
Rendimiento 36.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)c2cccc3c2nc(C(=O)NC2CCN(C(C)C)CC2)n3Cc2cc(-c3ccc(Cl)s3)on2)C1
Reaction #46840
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cnc1N1CC(Oc2cccc(F)c2)C1
Reaction #159620
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cccc(OC3CN(c4ncc(Cl)cc4C(=O)O)C3)c2)CC1
Reaction #159645
2-(3-(3-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenoxy)azetidin-1-yl)-5-chloronicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C(F)(F)F)cnc1N1CC(Oc2ccc(Cl)cc2)C1
Reaction #159654
title compound
Rendimiento 130.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C(F)(F)F)cnc1N1CC(Oc2cccc(Cl)c2)C1
Reaction #159655
title compound ( D124 )
Rendimiento 88.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4ccccc4)C3)CC2)cc1
Reaction #159671
title compound
Rendimiento 117.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](C)NC(=O)c2cc(Cl)cnc2N2CC(Oc3cccc(F)c3)C2)cc1
Reaction #159673
title compound ( D147 )
Rendimiento 80.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4ccc(C(F)(F)F)cc4)C3)CC2)cc1
Reaction #159674
title compound ( D148 )
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(C(F)(F)F)c4)C3)CC2)cc1
Reaction #159675
title compound ( D149 )
Rendimiento 8.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(F)c4)C3)CC2)cc1
Reaction #159677
title compound
Rendimiento 52.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(F)c4)C3)CC2)cc1
Reaction #159678
title compound
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(OC(F)(F)F)c4)C3)CC2)cc1
Reaction #159679
title compound ( D153 )
Rendimiento 75.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4ccc(F)cc4F)C3)CC2)cc1
Reaction #159680
title compound ( D154 )
Rendimiento 44.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4ccc(F)c(F)c4)C3)CC2)cc1
Reaction #159681
title compound ( D155 )
Rendimiento 38.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(N5CCN(C(=O)OC(C)(C)C)CC5)c4)C3)CC2)cc1
Reaction #159682
tert-butyl 4-(3-((1-(5-chloro-3-((1-(4-(methoxycarbonyl)phenyl)cyclopropyl)carbamoyl)pyridin-2-yl)azetidin-3-yl)oxy)phenyl)piperazine-1-carboxylate
Rendimiento 66.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(N5CCNCC5)c4)C3)CC2)cc1
Reaction #159683
title compound ( D156 )
Rendimiento 95.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CNC(=O)c2cc(Cl)cnc2N2CC(Oc3cccc(F)c3)C2)cc1
Reaction #159684
title compound ( D157 )
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CNC(=O)c2cc(Cl)cnc2N2CC(Oc3cccc(F)c3)C2)nc1
Reaction #159685
title compound ( D158 )
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(Oc4cccc(F)c4)C3)CC2)nc1
Reaction #159686
title compound ( D159 )
Rendimiento 24.2%DOI: 10.6084/m9.figshare.5104873.v1
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