BDBM50089095 CHEMBL216418::Met-Phe-Leu-Glu-Ala-Ile-Pro-Met-Ser-Ile
SMILES CC[C@@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@@H]1CCCN1C(=O)[C@H](NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](N)CCSC)[C@H](C)CC)C(O)=O
InChI Key InChIKey=KJFRMCLZOYOQQE-MODXBNNYSA-N
Data 3 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50089095
Affinity DataKi: 2.70E+4nMAssay Description:Competitive inhibition constant of the compound was tested against Human neutrophil elastase using the reporter substrate MeO-AAPV-pNaMore data for this Ligand-Target Pair
TargetChymotrypsin-like elastase family member 2A(Pig)
The Oxford Centre For Molecular Sciences
Curated by ChEMBL
The Oxford Centre For Molecular Sciences
Curated by ChEMBL
Affinity DataKi: 1.00E+5nMAssay Description:Peptide was tested for inhibition constant for competitive inhibition using Suc-AAPA-pNa and Pancreatic elastaseMore data for this Ligand-Target Pair
Affinity DataKi: 1.60E+5nMAssay Description:Competitive inhibition constant of the compound was tested against Chymotrypsinogen using the reporter substrate Suc-AAPA-pNaMore data for this Ligand-Target Pair