null

SMILES CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)O)C(=O)N[C@H](Cc2ccccc2)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@H](CCCCN)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(O)=O

InChI Key InChIKey=HFNHAPQMXICKCF-FDMLFMOBSA-N

  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 9 hits for monomerid = 50378580   

TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataKi:  0.794nMAssay Description:Displacement of [125I]urotensin-2 from human UT2 receptor expressed in CHO-K1 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27W6DFTPubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataKi:  0.794nMAssay Description:Binding affinity towards human Urotensin 2 receptor was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W9DS4PubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataKi:  0.794nMAssay Description:Ability to displace radioligand [125I]Tyr-hU-II from human recombinant Urotensin 2 receptor in CHO-K1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FR00C5PubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9ZTZPubMed
TargetUrotensin-2 receptor(RAT)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataEC50:  5.01nMAssay Description:Agonist activity at UT2 receptor in Albino rat aorta assessed as induction of aortic contractionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27W6DFTPubMed
TargetUrotensin-2 receptor(RAT)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataEC50:  0.832nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9ZTZPubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9ZTZPubMed
TargetUrotensin-2 receptor(RAT)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataEC50:  0.832nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9ZTZPubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50378580(CHEMBL437430)copy SMILEScopy InChI
Affinity DataEC50:  1.09nMAssay Description:Agonist activity at human GPR14 expressed in HEK293 cells by calcium mobilization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F47Q28PubMed