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TargetUrotensin-2 receptor
LigandBDBM50269953
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1707628 (CHEMBL4058861)
EC50 3.7±n/a nM
Citation Douchez, ABillard, EHébert, TEChatenet, DLubell, WD Design, Synthesis, and Biological Assessment of Biased Allosteric Modulation of the Urotensin II Receptor Using Achiral 1,3,4-Benzotriazepin-2-one Turn Mimics. J Med Chem60:9838-9859 (2017) [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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BDBM50269953
n/a
NameBDBM50269953
Synonyms:CHEMBL4103468
TypeSmall organic molecule
Emp. Form.C34H37ClN4O2
Mol. Mass.569.136
SMILESCl.COc1ccc(CCC2=NN(CCCCN)C(=O)N(Cc3ccc(cc3)-c3ccccc3)c3ccccc23)cc1 |t:8|
Structure
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