BDBM50120291 CHEMBL107869::Peptide Boronic Acid analogue

SMILES CC(C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](CCc1ccc(cc1)C(F)(F)F)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1

InChI Key InChIKey=IBYLOUOEHHNLIS-VJVHPBAHSA-N

Data  1 KI  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 3 hits for monomerid = 50120291   

TargetGenome polyprotein(Hepatitis C virus)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50120291(CHEMBL107869 | Peptide Boronic Acid analogue)
Affinity DataKi:  2nMAssay Description:Binding affinity against Hepatitis C virus NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50120291(CHEMBL107869 | Peptide Boronic Acid analogue)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibitory concentration against Human leukocyte ElastaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50120291(CHEMBL107869 | Peptide Boronic Acid analogue)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed