Teilstruktursuche

1209456

CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)N[C@H]3CCC[C@H]3C(=O)O)cc2F)C1
Reaction #88192
(1R,2S)-2-(6-((R)-3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinamido)cyclopentane-1-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3ccnc(C(=O)O)c3)cc2F)C1
Reaction #88195
(R)-4-((6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinamido)methyl)picolinic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(F)cnc3N3CC(Nc4ccc(F)cc4C)C3)CC2)cc1
Reaction #159711
title compound ( D190 )
Ausbeute 24.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1C(N)=O)c1ccc(F)cc1
Reaction #163041
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1CNS(C)(=O)=O)c1ccc(F)cc1
Reaction #163044
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163046
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163049
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(C#N)cc2F)n[nH]1
Reaction #163050
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(C(N)=O)cc2F)n[nH]1
Reaction #163051
title compound
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(CN)cc2F)n[nH]1
Reaction #163052
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(OC(C)C)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163053
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(CNS(C)(=O)=O)cc2F)n[nH]1
Reaction #163054
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(C#N)cc2F)n[nH]1
Reaction #163055
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(C(N)=O)cc2F)n[nH]1
Reaction #163056
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(OC(C)C)[nH]n2)nc1N[C@@H](C)c1ccc(F)cc1
Reaction #163058
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1C(=O)O)c1ccc(F)cc1
Reaction #163065
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(N(Cc2ccc(F)cc2)c2cc(C3CC3)[nH]n2)n1
Reaction #163067
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1CNC(=O)CN1CCOCC1)c1ccc(F)cc1
Reaction #163073
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1CN1CCOCC1)c1ccc(F)cc1
Reaction #163076
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](N)C(=O)NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](C)c1ccc(F)cc1
Reaction #163081
title compound
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter