Substructure Search

NCc1ccccc1

CN(C)C(c1cccc(Oc2ccccc2)c1)c1c(-c2ccc(F)cc2)[nH]c2ccccc12
Reaction #9173
[[2-(4-Fluoro-phenyl)-1H-indol-3-yl]-(3-phenoxy-phenyl)-methyl]-dimethyl-amine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #46654
(S)-benzyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)-2-(methoxycarbonylamino)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46655
gum
Yield 111.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](Cc1cn(Cc2ccccc2)nn1)C(=O)OCc1ccccc1
Reaction #49144
(S)-benzyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)-2-(methoxycarbonylamino)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49145
gum
Yield 111.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(c1ccccc1)n1ccc2cc(O)ccc21
Reaction #52283
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2c(=O)ccn([C@@H]3OC([C@H](O)[C@H](NCCCNC(=O)[C@@H](N)[C@H](C)O)C(=O)OC(C)(C)C)[C@@H](O)[C@H]3O)c2=O)cc1
Reaction #54015
tert-butyl (2S,3R)-2-[(3-{[(2S,3S)-2-amino-3-hydroxybutanoyl]amino}propyl)amino]-3-[(3S,4R,5R)-3,4-dihydroxy-5-(3-(4-methoxybenzyl)-2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl)-tetrahydro-2-furanyl]-3-hydroxypropanoate
Yield 92.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](NCCCC(=O)O)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56776
3-[2(R)-{hydroxycarbonylpropyl-amino}-2-phenylethyl]-5-(2-chlorophenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)C1=CN(C(=O)c2ccc(F)cc2)CCc2c1[nH]c1ccccc21
Reaction #66253
title compound
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(CO)cc2n1Cc1ccccc1
Reaction #68354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(C=O)cc2n1Cc1ccccc1
Reaction #68355
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(C(=O)NN)cc2n1Cc1ccccc1
Reaction #68373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(-c3nnco3)cc2n1Cc1ccccc1
Reaction #68374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(N)cc2n1Cc1ccccc1
Reaction #68400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(NC3CCOC3)cc2n1Cc1ccccc1
Reaction #68401
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)Nc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(N3CCCC3=O)cc2n1Cc1ccccc1
Reaction #68403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(NC3CCCC3)cc2n1Cc1ccccc1
Reaction #68404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(NC3=NCCO3)cc2n1Cc1ccccn1
Reaction #68430
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(N3CCCC3)cc2n1Cc1ccccn1
Reaction #68431
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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