Reaction Details |
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Target | Bombesin receptor subtype-3 |
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Ligand | BDBM50400254 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_872481 (CHEMBL2182521) |
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IC50 | 0.9±n/a nM |
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Citation | Liu, P; Lanza, TJ; Chioda, M; Jones, C; Chobanian, HR; Guo, Y; Chang, L; Kelly, TM; Kan, Y; Palyha, O; Guan, XM; Marsh, DJ; Metzger, JM; Ramsay, K; Wang, SP; Strack, AM; Miller, R; Pang, J; Lyons, K; Dragovic, J; Ning, JG; Schafer, WA; Welch, CJ; Gong, X; Gao, YD; Hornak, V; Ball, RG; Tsou, N; Reitman, ML; Wyvratt, MJ; Nargund, RP; Lin, LS Discovery of benzodiazepine sulfonamide-based bombesin receptor subtype 3 agonists and their unusual chirality. ACS Med Chem Lett2:933-937 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Bombesin receptor subtype-3 |
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Name: | Bombesin receptor subtype-3 |
Synonyms: | BRS-3 | BRS3 | BRS3_HUMAN | Bombesin 3 | Bombesin like receptor 3 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 44424.45 |
Organism: | Homo sapiens (Human) |
Description: | Bombesin 3 BRS3 HUMAN::P32247 |
Residue: | 399 |
Sequence: | MAQRQPHSPNQTLISITNDTESSSSVVSNDNTNKGWSGDNSPGIEALCAIYITYAVIISV
GILGNAILIKVFFKTKSMQTVPNIFITSLAFGDLLLLLTCVPVDATHYLAEGWLFGRIGC
KVLSFIRLTSVGVSVFTLTILSADRYKAVVKPLERQPSNAILKTCVKAGCVWIVSMIFAL
PEAIFSNVYTFRDPNKNMTFESCTSYPVSKKLLQEIHSLLCFLVFYIIPLSIISVYYSLI
ARTLYKSTLNIPTEEQSHARKQIESRKRIARTVLVLVALFALCWLPNHLLYLYHSFTSQT
YVDPSAMHFIFTIFSRVLAFSNSCVNPFALYWLSKSFQKHFKAQLFCCKAERPEPPVADT
SLTTLAVMGTVPGTGSIQMSEISVTSFTGCSVKQAEDRF
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BDBM50400254 |
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n/a |
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Name | BDBM50400254 |
Synonyms: | CHEMBL2179911 |
Type | Small organic molecule |
Emp. Form. | C24H24F3N3O2S |
Mol. Mass. | 475.526 |
SMILES | Cc1cccc2Nc3nc(ccc3CN(c12)S(=O)(=O)c1ccc(cc1)C(C)(C)C)C(F)(F)F |
Structure |
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