BDBM27884 4-{[(2S)-2-(3-chloro-4-methoxyphenyl)-2-hydroxyethyl]amino}-3-{6-[1-(3-fluoropropyl)piperidin-4-yl]-4-methyl-1H-1,3-benzodiazol-2-yl}-1,2-dihydropyridin-2-one::benzimidazole scaffold, 6

SMILES COc1ccc(cc1Cl)[C@H](O)CNc1cc[nH]c(=O)c1-c1nc2c(C)cc(cc2[nH]1)C1CCN(CCCF)CC1

InChI Key InChIKey=VSPZMUAUSBZZJK-RUZDIDTESA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 27884   

TargetCytochrome P450 3A4(Homo sapiens (Human))
Bristol-Myers Squibb

LigandPNGBDBM27884(4-{[(2S)-2-(3-chloro-4-methoxyphenyl)-2-hydroxyeth...)
Affinity DataIC50:  1.00E+4nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a dealkylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Befo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Bristol-Myers Squibb

LigandPNGBDBM27884(4-{[(2S)-2-(3-chloro-4-methoxyphenyl)-2-hydroxyeth...)
Affinity DataIC50:  20nMpH: 7.0 T: 2°CAssay Description:The IGF-1 receptor tyrosine kinase was assayed using the synthetic polymer poly(Glu/Tyr) as a phosphoacceptor substrate. Incorporated radioactivity w...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed