| Reaction Details |
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 | Report a problem with these data |
| Target | Histamine H3 receptor |
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| Ligand | BDBM50314312 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_624357 (CHEMBL1107887) |
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| Ki | 624±n/a nM |
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| Citation |  Berlin, M; Lee, YJ; Boyce, CW; Wang, Y; Aslanian, R; McCormick, KD; Sorota, S; Williams, SM; West, RE; Korfmacher, W Reduction of hERG inhibitory activity in the 4-piperidinyl urea series of H3 antagonists. Bioorg Med Chem Lett20:2359-64 (2010) [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 |
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| Synonyms: | G-protein coupled receptor 97 | GPCR97 | HH3R | HISTAMINE H3 | HRH3 | HRH3_HUMAN | Histamine H3 receptor (H3) | Histamine H3L | Histamine receptor (H3 and H4) |
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| Type: | G Protein-Coupled Receptor (GPCR) |
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| Mol. Mass.: | 48691.47 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Binding assays were using CHO cells stably expressing hH3R receptors. |
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| Residue: | 445 |
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| Sequence: | MERAPPDGPLNASGALAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCTS
SAFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMLLVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGAREAA
GPEPPPEAQPSPPPPPGCWGCWQKGHGEAMPLHRYGVGEAAVGAEAGEATLGGGGGGGSV
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSFTQRFRLSRDRKVAKSL
AVIVSIFGLCWAPYTLLMIIRAACHGHCVPDYWYETSFWLLWANSAVNPVLYPLCHHSFR
RAFTKLLCPQKLKIQPHSSLEHCWK
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| BDBM50314312 |
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| n/a |
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| Name | BDBM50314312 |
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| Synonyms: | 1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-((2-hydroxypyridin-4-yl)methyl)piperidin-4-yl)urea | CHEMBL1091835 |
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| Type | Small organic molecule |
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| Emp. Form. | C25H26ClFN4O2 |
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| Mol. Mass. | 468.951 |
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| SMILES | Fc1ccc(CNC(=O)N(C2CCN(Cc3cc[nH]c(=O)c3)CC2)c2ccc(Cl)cc2)cc1 |
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| Structure | 
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