BDBM50328532 (S)-1-(2-(5-(3-bromophenyl)-1H-imidazol-2-yl)-4,4-difluoropyrrolidin-1-yl)-3-(2',3'-dichlorobiphenyl-4-yl)-2,2-dimethylpropan-1-one::CHEMBL1259085

SMILES CC(C)(Cc1ccc(cc1)-c1cccc(Cl)c1Cl)C(=O)N1CC(F)(F)C[C@H]1c1nc(c[nH]1)-c1cccc(Br)c1

InChI Key InChIKey=LAVGXZGVOUSWFG-VWLOTQADSA-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 = 50328532   

TargetLysosomal Pro-X carboxypeptidase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50328532((S)-1-(2-(5-(3-bromophenyl)-1H-imidazol-2-yl)-4,4-...)
Affinity DataIC50:  22nMAssay Description:Inhibition of human PrCP by FRETMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal Pro-X carboxypeptidase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50328532((S)-1-(2-(5-(3-bromophenyl)-1H-imidazol-2-yl)-4,4-...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of human PrCP by FRET in presence of 1% mouse serum albuminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed