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TargetUrotensin-2 receptor
LigandBDBM50413047
Substrate/Competitorn/a
Meas. Tech.ChEMBL_496754 (CHEMBL1005391)
Ki 31.62±n/a nM
Citation Wang, YWu, ZGuida, BFLawrence, SKNeeb, MJRivero, RADouglas, SAJin, J N-alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists. Bioorg Med Chem Lett18:4936-9 (2008) [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 | GPR14 | UR-II-R | UR2R_HUMAN | UTS2R | Urotensin II receptor | Urotensin-II
Type:Enzyme Catalytic Domain
Mol. Mass.:42159.71
Organism:Homo sapiens (Human)
Description:Urotensin-II UTS2R HUMAN::Q9UKP6
Residue:389
Sequence:
MALTPESPSSFPGLAATGSSVPEPPGGPNATLNSSWASPTEPSSLEDLVATGTIGTLLSA
MGVVGVVGNAYTLVVTCRSLRAVASMYVYVVNLALADLLYLLSIPFIVATYVTKEWHFGD
VGCRVLFGLDFLTMHASIFTLTVMSSERYAAVLRPLDTVQRPKGYRKLLALGTWLLALLL
TLPVMLAMRLVRRGPKSLCLPAWGPRAHRAYLTLLFATSIAGPGLLIGLLYARLARAYRR
SQRASFKRARRPGARALRLVLGIVLLFWACFLPFWLWQLLAQYHQAPLAPRTARIVNYLT
TCLTYGNSCANPFLYTLLTRNYRDHLRGRVRGPGSGGGRGPVPSLQPRARFQRCSGRSLS
SCSPQPTDSLVLAPAAPARPAPEGPRAPA
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  Blast E-value cutoff:
BDBM50413047
n/a
NameBDBM50413047
Synonyms:CHEMBL497580
TypeSmall organic molecule
Emp. Form.C16H19N3O
Mol. Mass.269.3416
SMILESCCCCNc1ccnc2[nH]c3c(OC)cccc3c12
Structure
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