Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50071197 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_86899 |
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Ki | 56±n/a nM |
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Citation | Stark, H; Ligneau, X; Arrang, JM; Schwartz, JC; Schunack, W General construction pattern of histamine H3-receptor antagonists: change of a paradigm. Bioorg Med Chem Lett8:2011-6 (1999) [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 |
Synonyms: | HH3R | HRH3_RAT | Hrh3 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 48607.98 |
Organism: | Rattus norvegicus (rat) |
Description: | n/a |
Residue: | 445 |
Sequence: | MERAPPDGLMNASGTLAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCAS
SVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMALVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGREAG
PEPPPDAQPSPPPAPPSCWGCWPKGHGEAMPLHRYGVGEAGPGVEAGEAALGGGSGGGAA
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSL
AIIVSIFGLCWAPYTLLMIIRAACHGRCIPDYWYETSFWLLWANSAVNPVLYPLCHYSFR
RAFTKLLCPQKLKVQPHGSLEQCWK
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BDBM50071197 |
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n/a |
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Name | BDBM50071197 |
Synonyms: | 4-(4-Phenyl-butyl)-1H-imidazole | CHEMBL296450 |
Type | Small organic molecule |
Emp. Form. | C13H16N2 |
Mol. Mass. | 200.2795 |
SMILES | C(CCc1ccccc1)Cc1cnc[nH]1 |
Structure |
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