BDBM50328527 CHEMBL1259208::N-[(2S,3S)-1-[(2S)-2-(5,6-Dichloro-1H-benzimidazol-2-yl)-pyrrolidin-1-yl]-3-(4'-fluorobiphenyl-4-yl)-1-oxobutan-2-yl]-2-hydroxy-2-methylpropanamide

SMILES C[C@H]([C@H](NC(=O)C(C)(C)O)C(=O)N1CCC[C@H]1c1nc2cc(Cl)c(Cl)cc2[nH]1)c1ccc(cc1)-c1ccc(F)cc1

InChI Key InChIKey=SGBMSKHAEMUDTC-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50328527   

TargetLysosomal Pro-X carboxypeptidase(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50328527(N-[(2S,3S)-1-[(2S)-2-(5,6-Dichloro-1H-benzimidazol...)
Affinity DataIC50: 2nMAssay Description:Inhibition of human PrCP by FRETMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2011
Entry Details Article
PubMed
TargetLysosomal Pro-X carboxypeptidase(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50328527(N-[(2S,3S)-1-[(2S)-2-(5,6-Dichloro-1H-benzimidazol...)
Affinity DataIC50: 2nMAssay Description:Inhibition of human PrCP by FRET in presence of 1% mouse serum albuminMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2011
Entry Details Article
PubMed