Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetUrotensin-2 receptor
LigandBDBM50269957
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1707628 (CHEMBL4058861)
EC50 1.4±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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50269957
n/a
NameBDBM50269957
Synonyms:CHEMBL4068478
TypeSmall organic molecule
Emp. Form.C33H32ClN5OS
Mol. Mass.582.158
SMILESCl.NCCCN1N=C(CCc2nc3ccccc3s2)c2ccccc2N(Cc2ccc(cc2)-c2ccccc2)C1=O |t:5|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: