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TargetUrotensin-2 receptor
LigandBDBM50252354
Substrate/Competitorn/a
Meas. Tech.ChEMBL_487750 (CHEMBL1009482)
Ki 18±n/a nM
Citation Jin, JAn, MSapienza, AAiyar, NNaselsky, DSarau, HMFoley, JJSalyers, KLKnight, SDKeenan, RMRivero, RADhanak, DDouglas, SA Urotensin-II receptor antagonists: synthesis and SAR of N-cyclic azaalkyl benzamides. Bioorg Med Chem Lett18:3950-4 (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:
BDBM50252354
n/a
NameBDBM50252354
Synonyms:CHEMBL517991 | N-((S)-1-((S)-1-((R)-3-bromo-4-((R)-pyrrolidin-3-yloxy)phenethyl)pyrrolidin-3-ylamino)-4-methyl-1-oxopentan-2-yl)benzo[b]thiophene-2-carboxamide
TypeSmall organic molecule
Emp. Form.C31H39BrN4O3S
Mol. Mass.627.635
SMILESCC(C)C[C@H](NC(=O)c1cc2ccccc2s1)C(=O)N[C@H]1CCN(CCc2ccc(O[C@@H]3CCNC3)c(Br)c2)C1 |r|
Structure
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