Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50091373 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_86898 (CHEMBL698408) |
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Ki | 0.3±n/a nM |
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Citation | Sasse, A; Sadek, B; Ligneau, X; Elz, S; Pertz, HH; Luger, P; Ganellin, CR; Arrang, JM; Schwartz, JC; Schunack, W; Stark, H New histamine H(3)-receptor ligands of the proxifan series: imoproxifan and other selective antagonists with high oral in vivo potency. J Med Chem43:3335-43 (2000) [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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BDBM50091373 |
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n/a |
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Name | BDBM50091373 |
Synonyms: | 1-{2-Fluoro-4-[3-(1H-imidazol-4-yl)-propoxy]-phenyl}-ethanone oxime; compound with but-2-enedioic acid | CHEMBL321835 |
Type | Small organic molecule |
Emp. Form. | C14H16FN3O2 |
Mol. Mass. | 277.2941 |
SMILES | CC(N=O)c1ccc(OCCCc2cnc[nH]2)cc1F |
Structure |
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