BDBM50228894 CHEMBL312754

SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O

InChI Key InChIKey=XIEWFECSPPTVQN-UHFFFAOYSA-N

Data  3 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 = 50228894   

LigandPNGBDBM50228894(CHEMBL312754)
Affinity DataIC50: 1.60nMAssay Description:Binding affinity against Angiotensin II receptor, from rat adrenal glandMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/28/2019
Entry Details Article
PubMed
LigandPNGBDBM50228894(CHEMBL312754)
Affinity DataIC50: 5.10nMAssay Description:Binding affinity for rat brain Angiotensin II receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/28/2019
Entry Details Article
PubMed
TargetType-1/Type-2 angiotensin II receptor(Human)
Berlex Laboratories

Curated by ChEMBL
LigandPNGBDBM50228894(CHEMBL312754)
Affinity DataIC50: 5.80nMAssay Description:Inhibitory activity as antagonist of AII on guinea pig ileumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2019
Entry Details Article
PubMed