BDBM50445373 CHEMBL3104461

SMILES CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](C)N)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H]2Cc3c(CN([C@@H](CCCCN)C(=O)N[C@@H](Cc4ccc(O)cc4)C(=O)N1)C2=O)[nH]c1ccccc31)C(O)=O

InChI Key InChIKey=QFXBKPNJQYMVFO-UHFFFAOYSA-N

Data  2 IC50  2 EC50

  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 4 hits for monomerid = 50445373   

TargetUrotensin-2 receptor(Human)
Laval University

Curated by ChEMBL
LigandPNGBDBM50445373(CHEMBL3104461)
Affinity DataIC50: 60nMAssay Description:Displacement of [125I]-Urotensin-2 from human GPR14 expressed in CHO cells after 90 mins by gamma counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetUrotensin-2 receptor(Human)
Laval University

Curated by ChEMBL
LigandPNGBDBM50445373(CHEMBL3104461)
Affinity DataIC50: 60nMAssay Description:Displacement of [125I]-Urotensin-2 from human GPR14 expressed in CHO cells after 90 mins by gamma counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetUrotensin-2 receptor(Rat)
Laval University

Curated by ChEMBL
LigandPNGBDBM50445373(CHEMBL3104461)
Affinity DataEC50:  159nMAssay Description:Agonist activity at urotensin-2 receptor in Sprague-Dawley rat aortic rings assessed as KCl-induced vasoconstrictionMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetUrotensin-2 receptor(Rat)
Laval University

Curated by ChEMBL
LigandPNGBDBM50445373(CHEMBL3104461)
Affinity DataEC50:  162nMAssay Description:Agonist activity at urotensin-2 receptor in Sprague-Dawley rat aortic rings assessed as KCl-induced vasoconstrictionMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed