Reaction Details |
| Report a problem with these data |
Target | Urotensin-2 receptor |
---|
Ligand | BDBM50252354 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_487750 (CHEMBL1009482) |
---|
Ki | 18±n/a nM |
---|
Citation | Jin, J; An, M; Sapienza, A; Aiyar, N; Naselsky, D; Sarau, HM; Foley, JJ; Salyers, KL; Knight, SD; Keenan, RM; Rivero, RA; Dhanak, D; Douglas, 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
|
|
|
BDBM50252354 |
---|
n/a |
---|
Name | BDBM50252354 |
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 |
Type | Small organic molecule |
Emp. Form. | C31H39BrN4O3S |
Mol. Mass. | 627.635 |
SMILES | CC(C)C[C@H](NC(=O)c1cc2ccccc2s1)C(=O)N[C@H]1CCN(CCc2ccc(O[C@@H]3CCNC3)c(Br)c2)C1 |r| |
Structure |
|