Reaction Details |
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Target | Urotensin-2 receptor |
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Ligand | BDBM50459262 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1766053 (CHEMBL4201300) |
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EC50 | 1.1±n/a nM |
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Citation | Billard, E; Hébert, TE; Chatenet, D Discovery of New Allosteric Modulators of the Urotensinergic System through Substitution of the Urotensin II-Related Peptide (URP) Phenylalanine Residue. J Med Chem61:8707-8716 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Urotensin-2 receptor |
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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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BDBM50459262 |
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n/a |
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Name | BDBM50459262 |
Synonyms: | CHEMBL4213538 |
Type | Small organic molecule |
Emp. Form. | C50H63IN10O12S2 |
Mol. Mass. | 1187.129 |
SMILES | CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](N)CC(O)=O)C(=O)N[C@@H](Cc2ccc(I)cc2)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(O)=O |r| |
Structure |
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