Reaction Details |
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Target | Histamine receptor H3 |
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Ligand | BDBM50158601 |
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Substrate/Competitor | n/a |
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Ki | 4.27±n/a nM |
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Comments | PDSP_2991 |
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Citation | Esbenshade, TA; Krueger, KM; Miller, TR; Kang, CH; Denny, LI; Witte, DG; Yao, BB; Fox, GB; Faghih, R; Bennani, YL; Williams, M; Hancock, AA Two novel and selective nonimidazole histamine H3 receptor antagonists A-304121 and A-317920: I. In vitro pharmacological effects. J Pharmacol Exp Ther305:887-96 (2003) [PubMed] Article |
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More Info.: | Get all data from this article |
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Histamine receptor H3 |
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Name: | Histamine receptor H3 |
Synonyms: | HISTAMINE H3 | HRH3 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 16901.59 |
Organism: | Dog |
Description: | Q865E3 |
Residue: | 147 |
Sequence: | FLLNLAISDFLVGAFCIPLYVPYVLTGRWPFSRGLCKLWLVVDYLLCTSSVFNIVLISYD
RFLSVTRAVSYRAQQGDTRRAVQKMVLVWVLAFLLYGPAILSWEHLSGGSSIPEGHCYAE
FFYNWYFLITASTLEFFTPFLSVTFFN
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BDBM50158601 |
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n/a |
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Name | BDBM50158601 |
Synonyms: | A-317920 | CHEMBL361355 | Furan-2-carboxylic acid ((R)-2-{4-[3-(4-cyclopropanecarbonyl-phenoxy)-propyl]-piperazin-1-yl}-1-methyl-2-oxo-ethyl)-amide |
Type | Small organic molecule |
Emp. Form. | C25H31N3O5 |
Mol. Mass. | 453.5307 |
SMILES | C[C@@H](NC(=O)c1ccco1)C(=O)N1CCN(CCCOc2ccc(cc2)C(=O)C2CC2)CC1 |
Structure |
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