BDBM50022005 Ac-His-Pro-Phe-His-Statine-Leu-Phe-NH2::CHEMBL266410

SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(C)=O)[C@@H](O)CC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key InChIKey=SBISAPJFLPILLA-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 = 50022005   

TargetRenin(Rat)
Massachusetts General Hospital

Curated by ChEMBL
LigandPNGBDBM50022005(CHEMBL266410 | Ac-His-Pro-Phe-His-Statine-Leu-Phe-...)
Affinity DataIC50: 210nMAssay Description:Inhibitory activity against rat plasma renin in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/17/2012
Entry Details Article
PubMed
TargetRenin(Human)
Massachusetts General Hospital

Curated by ChEMBL
LigandPNGBDBM50022005(CHEMBL266410 | Ac-His-Pro-Phe-His-Statine-Leu-Phe-...)
Affinity DataIC50: 14nMAssay Description:Compound was tested for its inhibitory activity against human plasma reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/17/2012
Entry Details Article
PubMed