| Reaction Details |
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 | Report a problem with these data |
| Target | Bombesin receptor subtype-3 |
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| Ligand | BDBM50381918 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_817747 (CHEMBL2027395) |
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| IC50 | 0.5±n/a nM |
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| Citation |  Chobanian, HR; Guo, Y; Liu, P; Lanza, TJ; Chioda, M; Chang, L; Kelly, TM; Kan, Y; Palyha, O; Guan, XM; Marsh, DJ; Metzger, JM; Raustad, K; Wang, SP; Strack, AM; Gorski, JN; Miller, R; Pang, J; Lyons, K; Dragovic, J; Ning, JG; Schafer, WA; Welch, CJ; Gong, X; Gao, YD; Hornak, V; Reitman, ML; Nargund, RP; Lin, LS The design and synthesis of potent, selective benzodiazepine sulfonamide bombesin receptor subtype 3 (BRS-3) agonists with an increased barrier of atropisomerization. Bioorg Med Chem20:2845-9 (2012) [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 |
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| Synonyms: | BRS-3 | BRS3 | BRS3_HUMAN | Bombesin 3 | Bombesin like receptor 3 |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 44424.45 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Bombesin 3 BRS3 HUMAN::P32247 |
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| Residue: | 399 |
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| Sequence: | MAQRQPHSPNQTLISITNDTESSSSVVSNDNTNKGWSGDNSPGIEALCAIYITYAVIISV
GILGNAILIKVFFKTKSMQTVPNIFITSLAFGDLLLLLTCVPVDATHYLAEGWLFGRIGC
KVLSFIRLTSVGVSVFTLTILSADRYKAVVKPLERQPSNAILKTCVKAGCVWIVSMIFAL
PEAIFSNVYTFRDPNKNMTFESCTSYPVSKKLLQEIHSLLCFLVFYIIPLSIISVYYSLI
ARTLYKSTLNIPTEEQSHARKQIESRKRIARTVLVLVALFALCWLPNHLLYLYHSFTSQT
YVDPSAMHFIFTIFSRVLAFSNSCVNPFALYWLSKSFQKHFKAQLFCCKAERPEPPVADT
SLTTLAVMGTVPGTGSIQMSEISVTSFTGCSVKQAEDRF
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| BDBM50381918 |
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| n/a |
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| Name | BDBM50381918 |
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| Synonyms: | CHEMBL2023113 |
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| Type | Small organic molecule |
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| Emp. Form. | C25H20F6N4O4S |
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| Mol. Mass. | 586.506 |
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| SMILES | NC(=O)C1(CCC1)c1cccc2Nc3nc(ccc3CN(c12)S(=O)(=O)c1ccc(OC(F)(F)F)cc1)C(F)(F)F |
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| Structure | 
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