Reaction Details |
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Target | Urotensin-2 receptor |
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Ligand | BDBM50302264 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_596665 (CHEMBL1048827) |
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IC50 | 2±n/a nM |
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Citation | Lawson, EC; Luci, DK; Ghosh, S; Kinney, WA; Reynolds, CH; Qi, J; Smith, CE; Wang, Y; Minor, LK; Haertlein, BJ; Parry, TJ; Damiano, BP; Maryanoff, BE Nonpeptide urotensin-II receptor antagonists: a new ligand class based on piperazino-phthalimide and piperazino-isoindolinone subunits. J Med Chem52:7432-45 (2009) [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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BDBM50302264 |
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n/a |
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Name | BDBM50302264 |
Synonyms: | (R)-N-(4-(3,4-dimethoxyphenyl)-4-(4-(4-isopropylpiperazin-1-yl)-1-oxoisoindolin-2-yl)butyl)-N-methylthiophene-2-sulfonamide | CHEMBL578203 |
Type | Small organic molecule |
Emp. Form. | C32H42N4O5S2 |
Mol. Mass. | 626.83 |
SMILES | COc1ccc(cc1OC)[C@@H](CCCN(C)S(=O)(=O)c1cccs1)N1Cc2c(cccc2N2CCN(CC2)C(C)C)C1=O |r| |
Structure |
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