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11451

CCCCN(C)Cc1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(C(C)C)c2)c1.Cl.Cl
Reaction #42395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](CC2CCCCC2)[C@H](O)CNCc2cccc(Br)c2)c1.Cl
Reaction #42555
N1-[(1S,2R)-3-[(3-bromobenzyl)amino]-1-(cyclohexylmethyl)-2-hydroxypropyl]-5-methyl-N3,N3-dipropylisophthalamide hydrochloride
Ausbeute 38.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49233
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49240
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N(CCC)CCC)c2)C1
Reaction #49241
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(N2CCN(C(=O)c3cc(C#N)ccc3N3CCOCC3)CC2)c(F)c1
Reaction #61002
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(O)c(-c2ccccc2)c1
Reaction #70334
5-Cyclopropyl-2-(6-hydroxy-5-phenylpyridin-3-ylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccc(Cl)cc1)[C@H]1CCCC[C@@H]1NC(=O)CNC(=O)c1cccc(C(F)(F)F)c1.NC(=O)c1ccccc1
Reaction #77831
benzamide N-[2-[[(1S,2S)-2-[(4-chlorobenzyl)(methyl)amino]cyclohexyl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamide
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2ccc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(C#N)cn2)c1
Reaction #89333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(C#N)cn2)c1
Reaction #89335
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc3ccccc3n2)c1
Reaction #89436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(C(F)(F)F)cn2)c1F
Reaction #89531
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(-c2ccccc2)ccc1C(=O)O)c1cc(-c2ccccc2)ccc1O
Reaction #190584
DOI: 10.1039/C8SC04228D
O=C(CNC(=O)c1cccc(C(F)(F)F)c1)NC1CCN(C2CCN(c3ccccc3F)CC2)C1
Reaction #191240
DOI: 10.1039/C8SC04228D
O=C(CNC(=O)c1cccc(C(F)(F)F)c1)NCC1CCN(Cc2ccc(NC(=O)c3ccccc3)cc2)CC1
Reaction #194037
DOI: 10.1039/C8SC04228D
CN1CCC(c2ccc(O)c(C(=O)Nc3cc(-c4ccccc4)ccc3C(=O)O)c2)CC1
Reaction #198128
DOI: 10.1039/C8SC04228D
Cc1cccc(N2CCC(N3CCC(NC(=O)CNC(=O)c4cccc(C(F)(F)F)c4)C3)CC2)c1
Reaction #199886
DOI: 10.1039/C8SC04228D
N#Cc1cccc(C(=O)n2c(-c3cccnc3)cc3cc(C#N)ccc32)c1
Reaction #202865
DOI: 10.1039/C8SC04228D
Cc1cccc(C(=O)NC(Nc2c(Nc3cccnc3)c(=O)c2=O)C(C)(C)Cc2ccncc2)c1
Reaction #209536
DOI: 10.1039/C8SC04228D
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