Busqueda de Subestructura

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CC[C@@H](C(=O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H]1O[C@@H](CC(=O)OO)[C@H](C)C[C@@H]1C)[C@H]1O[C@](C)([C@]2(O)O[C@](CC)([C@@H](O)CC)C[C@H]2C)C[C@@H]1C
Reaction #62575
lysocellin
DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(N3CC4CCOC4(CN)C3)c(F)cc3c(=O)c(C(=O)O)cn1c23.Cl
Reaction #82166
10-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]oct-7-yl)-9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C[C@H]2CCCO2)C(=O)OC(C)(C)C)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85050
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[(2R)-tetrahydrofuran-2-yl]propanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C[C@H]2CCCO2)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85051
2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[(2R)-tetrahydrofuran-2-yl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C[C@@H]2CCCO2)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85053
2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[(2S)-tetrahydrofuran-2-yl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(=CC2CCOC2)C(=O)OC(C)(C)C)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85055
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(tetrahydrofuran-3-yl)acrylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(CC2CCOC2)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85056
2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(tetrahydrofuran-3-yl)propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(/C=C/CC(C)CCCC(C)(C)OC)=C1COC(=O)C1
Reaction #95403
aimed compound
Rendimiento 52.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)CCCC(C)C/C=C/C(=O)C1COC(=O)C1
Reaction #95404
aimed compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(/C=C(/O)CC(C)CCCC(C)(C)OC)=C1COC(=O)C1
Reaction #95405
aimed compound
Rendimiento 63.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(C(=O)c1ccc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1C)C1CCCO1
Reaction #175774
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(CC2CCOC2)COC1(C)C
Reaction #181448
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C1CC(Cc2ccc(-c3ccccn3)cc2)C(=O)O1
Reaction #189376
DOI: 10.1039/C8SC04228D
CC(C)(C)C(NC(=O)c1ccc(N)c(Cl)c1)C(=O)N1CCCC1C(=O)NC1CC(=O)OC1OCc1ccccc1
Reaction #190103
DOI: 10.1039/C8SC04228D
CC1CCC(N(C(=O)C2CCCO2)C2CC(C(=O)N3CCN(C)CC3)N(C(=O)C3CN(C(=O)OC(C)(C)C)CC3c3ccc(Cl)cc3)C2)CC1
Reaction #190218
DOI: 10.1039/C8SC04228D
CC(C)(O)CCC(CC(O)C(Cc1cccc(F)c1)NC(=O)c1cnc2ccccc2n1)C(N)=O
Reaction #194915
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1=NC2(c3cc(NC4CCCC4)ccc3F)OCCC2CS1
Reaction #198533
DOI: 10.1039/C8SC04228D
CN1COc2c(N3CC4CCOC4(CNC(=O)OC(C)(C)C)C3)c(F)cc3c(=O)c(C(=O)O)cn1c23
Reaction #206272
DOI: 10.1039/C8SC04228D
CCC(=O)OC1C(COC(C)=O)OC(n2cc3[nH]c(=O)c4c(=O)[nH]ncc(n2)c34)C1OC(C)=O
Reaction #227975
DOI: 10.1039/C8SC04228D
Cc1nc(OCC(=O)N(C)C2CCN(CC3CCCO3)CC2)nc(C)c1NC(=O)OC(C)(C)C
Reaction #229988
DOI: 10.1039/C8SC04228D
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