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TargetUrotensin-2 receptor
LigandBDBM50089660
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1496205 (CHEMBL3579089)
EC50 1.5±n/a nM
Citation Dufour-Gallant, JChatenet, DLubell, WD De Novo Conception of Small Molecule Modulators Based on Endogenous Peptide Ligands: Pyrrolodiazepin-2-oneż-Turn Mimics That Differentially Modulate Urotensin II Receptor-Mediated Vasoconstriction ex Vivo. J Med Chem58:4624-37 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Urotensin-2 receptor
Name:Urotensin-2 receptor
Synonyms:G-protein coupled receptor 14 | G-protein coupled sensory epithelial neuropeptide-like receptor | Gpr14 | Senr | UR-II-R | UR2R_RAT | Urotensin-II | Uts2r
Type:Enzyme Catalytic Domain
Mol. Mass.:42725.34
Organism:RAT
Description:Urotensin-II UTS2R RAT::P49684
Residue:386
Sequence:
MALSLESTTSFHMLTVSGSTVTELPGDSNVSLNSSWSGPTDPSSLKDLVATGVIGAVLSA
MGVVGMVGNVYTLVVMCRFLRASASMYVYVVNLALADLLYLLSIPFIIATYVTKDWHFGD
VGCRVLFSLDFLTMHASIFTLTIMSSERYAAVLRPLDTVQRSKGYRKLLVLGTWLLALLL
TLPMMLAIQLVRRGSKSLCLPAWGPRAHRTYLTLLFGTSIVGPGLVIGLLYVRLARAYWL
SQQASFKQTRRLPNPRVLYLILGIVLLFWACFLPFWLWQLLAQYHEAMPLTPETARIVNY
LTTCLTYGNSCINPFLYTLLTKNYREYLRGRQRSLGSSCHSPGSPGSFLPSRVHLQQDSG
RSLSSSSQQATETLMLSPVPRNGALL
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  Blast E-value cutoff:
BDBM50089660
n/a
NameBDBM50089660
Synonyms:CHEMBL3577311
TypeSmall organic molecule
Emp. Form.C30H32N4O4
Mol. Mass.512.5995
SMILESNCCCC[C@@H]1N[C@H](c2[nH]c(cc2N(CCc2ccc(O)cc2)C1=O)C(O)=O)c1ccc2ccccc2c1 |r|
Structure
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