null

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](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(C)(C)C)C(O)=O

InChI Key InChIKey=PHHPOPBJNOMNPB-UFPWOEGQSA-N

  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 = 50445386   

TargetUrotensin-2 receptor(Homo sapiens (Human))
Universit£ du Qu£bec

Curated by ChEMBL
LigandPNGBDBM50445386(CHEMBL3104641)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay 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(Homo sapiens (Human))
Universit£ du Qu£bec

Curated by ChEMBL
LigandPNGBDBM50445386(CHEMBL3104641)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay 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