BDBM50328531 3-(Biphenyl-4-yl)-1-{2-[5-(3-fluorophenyl)-1H-imidazol-2-yl]-pyrrolidin-1-yl}-2,2-dimethylpropan-1-one::CHEMBL1259069
SMILES: CC(C)(Cc1ccc(cc1)-c1ccccc1)C(=O)N1CCC[C@H]1c1nc(c[nH]1)-c1cccc(F)c1
InChI Key: InChIKey=RMEWBPGDAAPWCD-MHZLTWQESA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Prolylcarboxypeptidase (PRCP) (Homo sapiens (Human)) | BDBM50328531 (3-(Biphenyl-4-yl)-1-{2-[5-(3-fluorophenyl)-1H-imid...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 79 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human PrCP by FRET | J Med Chem 53: 7251-63 (2010) Article DOI: 10.1021/jm101013m BindingDB Entry DOI: 10.7270/Q2QV3MQR | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prolylcarboxypeptidase (PRCP) (Homo sapiens (Human)) | BDBM50328531 (3-(Biphenyl-4-yl)-1-{2-[5-(3-fluorophenyl)-1H-imid...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.46E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human PrCP by FRET in presence of 1% mouse serum albumin | J Med Chem 53: 7251-63 (2010) Article DOI: 10.1021/jm101013m BindingDB Entry DOI: 10.7270/Q2QV3MQR | |||||||||||
More data for this Ligand-Target Pair |