BDBM50472359 CHEMBL411733

SMILES [H][C@]12CC[C@H](N1C(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCS2)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(O)=O

InChI Key InChIKey=YWZYDGNGSXZELD-UHFFFAOYSA-N

Data  1 KI  1 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 2 hits for monomerid = 50472359   

TargetType-1 angiotensin II receptor A/B(Rat)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50472359(CHEMBL411733)
Affinity DataIC50: 800nMAssay Description:In vitro inhibitory activity against rat Angiotensin II receptor, type 1 expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2020
Entry Details Article
PubMed
TargetType-1 angiotensin II receptor A/B(Rat)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50472359(CHEMBL411733)
Affinity DataKi:  750nMAssay Description:In vitro binding affinity against Angiotensin II receptor, type 1 from rat liver membranesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2020
Entry Details Article
PubMed