| Reaction Details |
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 | Report a problem with these data |
| Target | Histamine H3 receptor |
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| Ligand | BDBM50092833 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEBML_83643 |
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| Ki | 27±n/a nM |
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| Citation |  Stark, H; Sippl, W; Ligneau, X; Arrang, JM; Ganellin, CR; Schwartz, JC; Schunack, W Different antagonist binding properties of human and rat histamine H3 receptors. Bioorg Med Chem Lett11:951-4 (2001) [PubMed] |
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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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| BDBM50092833 |
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| n/a |
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| Name | BDBM50092833 |
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| Synonyms: | 4-(3-Phenoxy-propyl)-1H-imidazole with (0.95M)oxalic acid | CHEMBL112951 | CHEMBL128923 |
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| Type | Small organic molecule |
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| Emp. Form. | C12H14N2O |
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| Mol. Mass. | 202.2524 |
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| SMILES | C(COc1ccccc1)Cc1cnc[nH]1 |
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| Structure | 
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