Recherche de Sous-structure

2730

CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #663
Rendement 35.1%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #664
Rendement 53.6%
CC1(C)Cc2c(-c3cc(NC(=O)[C@@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #743
Rendement 84.4%
COC(=O)C1(c2ccc(F)c(F)c2)Oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2C1=O
Reaction #8898
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1c(-c2ccc(F)c(F)c2)oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #8899
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1nc(-c2ccc(F)cc2)c(-c2ccncc2)[nH]1
Reaction #75040
title compound
Rendement 15.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4C3CC3)CC1CCO2
Reaction #82160
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]-oct-7-yl)-1-cyclopropyl-6-fluoro-1,4 -dihydro-4 -oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3c(F)cc4c(=O)c(C(=O)O)cn([C@@H]5C[C@@H]5F)c4c3F)CC1CCO2
Reaction #82162
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]-oct-7-yl)-6,8-difluoro-1-(cis-2-fluorocyclopropyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CC4CCOC4(CN)C3)c(F)c21.Cl
Reaction #82164
7-(1-aminomethyl-2-oxa-7-azabicyclo[3.3.0]oct-7-yl)-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2c(-c3ccncc3)nn3nccnc23)cc1
Reaction #83221
8-(4-fluorophenyl)-7-(pyridin-4-yl)pyrazolo[1,5-b][1,2,4]triazine
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4c[nH]nn4)ccc32)c1
Reaction #92434
N-(5-(5-(1H-1,2,3-triazol-4-yl)-1H-benzo[d]imidazol-1-yl)-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Rendement 2.3%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4c[nH]nn4)cnc32)c1
Reaction #92439
N-(5-(6-(1H-1,2,3-triazol-4-yl)-3H-imidazo[4,5-b]pyridin-3-yl)-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Rendement 9.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3=O
Reaction #156522
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3
Reaction #156523
title compound
Rendement 13.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCN(c3cccnc3)C2=O)sc2ccc(F)cc12
Reaction #167209
product
Rendement 61.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2sc3ccc(F)cc3c2C)C1=O
Reaction #167238
product
Rendement 60.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCN(c3ccc4ncsc4c3)C2=O)cncc1C(F)(F)F.O=C(O)C(F)(F)F
Reaction #167438
product
Rendement 3.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C(=O)NCC(O)C(F)(F)F)c(-n2c(C)ccc2C)cc1C(F)(F)F
Reaction #174352
DOI: 10.1039/C8SC04228D
Cc1cc(C(=O)Nc2cccc(Oc3ccc4nc(NC(=O)C5CC5)nn4c3)c2)n(CC(F)(F)F)n1
Reaction #177091
DOI: 10.1039/C8SC04228D
O=C(O)CCCC(=O)N1CCN(c2cc3c(cc2F)c(=O)c(C(=O)O)c2sccn23)CC1
Reaction #180222
DOI: 10.1039/C8SC04228D
Page 1Suivant