部分構造検索

1215081

CCCCCCCN(CCc1ccc(NC(C)(C)C(=O)O)cc1)C(=O)Nc1ccc(F)cc1F
Reaction #76109
2-(4-{2-[3-(2,4-difluoro-phenyl)-1-heptyl-ureido]-ethyl}-phenylamino)-2-methyl-propionic acid
収率 8.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(N[C@H](Cc2ccc(-n3ccnc3)cc2)C(N)=O)cc1Br
Reaction #172084
(R)-3-(4-(1H-imidazol-1-yl)phenyl)-2-(5-bromo-4-cyano-2-fluorophenylamino)propanamide
収率 31.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](Cc3ccc(-n4ccnc4)cc3)C(N)=O)c(F)cc2C#N)sn1
Reaction #172085
(R)-3-(4-(1H-imidazol-1-yl)phenyl)-2-(4-cyano-2-fluoro-5-(3-methylisothiazol-5-ylamino)phenylamino)propanamide
収率 14.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc3c(c2)NC(=O)C(C)(c2ccc([N+](=O)[O-])cc2)C3=O)CC1
Reaction #176202
DOI: 10.1039/C8SC04228D
COc1cc2c(c(OC)c1OC)CN(CCc1ccc([N+](=O)[O-])cc1)CC2
Reaction #181875
DOI: 10.1039/C8SC04228D
CN1CCc2cc(Cl)c(NC=O)cc2C(c2ccccc2)C1
Reaction #191217
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Nc2cc3c(cc2[N+](=O)[O-])NC(=O)C3(C)C)cc1
Reaction #199952
DOI: 10.1039/C8SC04228D
CC1CCCN1CCc1ccc(N)c(C=O)c1
Reaction #204929
DOI: 10.1039/C8SC04228D
Cc1ccc(CCCNC(=O)N2CCC(Nc3ccc(CCNCC(O)COc4ccc(O)cc4)cc3)CC2)cc1
Reaction #205315
DOI: 10.1039/C8SC04228D
CCC(=O)N(c1ccccc1)C1(COC)CCN(CCc2ccc([N+](=O)[O-])cc2)CC1
Reaction #211111
DOI: 10.1039/C8SC04228D
Cl.Nc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #216144
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@H]2COC(=O)N2)cc1
Reaction #216145
desired product
収率 114.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C[C@@H]2COC(=O)N2)cc1
Reaction #216159
desired product
収率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1cc(C)c(NC(=O)OC(C)(C)C)cc1CCl)NC(=O)OCc1ccccc1
Reaction #219363
Title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1cc(C)c(NC(=O)OC(C)(C)C)cc1CCl)NC(=O)OCc1ccccc1
Reaction #219497
Title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1cc(C)c(NC(=O)OC(C)(C)C)cc1CCl)NC(=O)OCc1ccccc1
Reaction #219599
Title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN(CCc1ccc(NC(C)(C)C(=O)O)cc1)C(=O)Nc1ccc(F)cc1F
Reaction #225033
DOI: 10.1039/C8SC04228D
CNC(=O)c1ccccc1Nc1nc(Nc2cc3c(cc2OC)CCN(CCN2CCOCC2)CC3)ncc1Cl
Reaction #231170
DOI: 10.1039/C8SC04228D
CCc1nc(-c2cccc(C)n2)cn1-c1ccc(CCNC(=O)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #237225
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1ccc(CCN2CCOc3ccc(-n4ccnc4)cc3OCC2)cc1
Reaction #243483
DOI: 10.1039/C8SC04228D
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