Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50410342 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_304030 (CHEMBL840208) |
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Ki | 0.447±n/a nM |
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Citation | Dvorak, CA; Apodaca, R; Barbier, AJ; Berridge, CW; Wilson, SJ; Boggs, JD; Xiao, W; Lovenberg, TW; Carruthers, NI 4-phenoxypiperidines: potent, conformationally restricted, non-imidazole histamine H3 antagonists. J Med Chem48:2229-38 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histamine H3 receptor |
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Name: | Histamine H3 receptor |
Synonyms: | G-protein coupled receptor 97 | GPCR97 | HH3R | HISTAMINE H3 | HRH3 | HRH3_HUMAN | Histamine H3 receptor (H3) | Histamine H3L | Histamine receptor (H3 and H4) |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 48691.47 |
Organism: | Homo sapiens (Human) |
Description: | Binding assays were using CHO cells stably expressing hH3R receptors. |
Residue: | 445 |
Sequence: | MERAPPDGPLNASGALAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCTS
SAFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMLLVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGAREAA
GPEPPPEAQPSPPPPPGCWGCWQKGHGEAMPLHRYGVGEAAVGAEAGEATLGGGGGGGSV
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSFTQRFRLSRDRKVAKSL
AVIVSIFGLCWAPYTLLMIIRAACHGHCVPDYWYETSFWLLWANSAVNPVLYPLCHHSFR
RAFTKLLCPQKLKIQPHSSLEHCWK
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BDBM50410342 |
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n/a |
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Name | BDBM50410342 |
Synonyms: | CHEMBL195408 |
Type | Small organic molecule |
Emp. Form. | C16H18N2O |
Mol. Mass. | 254.3269 |
SMILES | C[C@@H]1CCCN1CCc1cc2cc(ccc2o1)C#N |
Structure |
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