Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50177551 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_334179 (CHEMBL866473) |
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Ki | 4±n/a nM |
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Citation | Berlin, M; Ting, PC; Vaccaro, WD; Aslanian, R; McCormick, KD; Lee, JF; Albanese, MM; Mutahi, MW; Piwinski, JJ; Shih, NY; Duguma, L; Solomon, DM; Zhou, W; Sher, R; Favreau, L; Bryant, M; Korfmacher, WA; Nardo, C; West, RE; Anthes, JC; Williams, SM; Wu, RL; Susan She, H; Rivelli, MA; Corboz, MR; Hey, JA Reduction of CYP450 inhibition in the 4-[(1H-imidazol-4-yl)methyl]piperidine series of histamine H3 receptor antagonists. Bioorg Med Chem Lett16:989-94 (2006) [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: | HISTAMINE H3 | HRH3 | HRH3_CAVPO | Histamine H3 receptor |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 48753.61 |
Organism: | GUINEA PIG |
Description: | HISTAMINE H3 HRH3 GUINEA PIG::Q9JI35 |
Residue: | 445 |
Sequence: | MERAPPDGLMNASGALAGEAAAAAGGARTFSAAWTAVLAALMALLIVATVLGNALVMLAF
VADSSLRTQNNFFLLNLAISDFLVGVFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCT
SSVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMVLVWVLAFLLYGPAILSWEYLSG
GSSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGARE
AGPDPLPEAQSSPPQPPPGCWGCWPKGQGESMPLHRYGVGEAGPGAEAGEAALGGGSGAA
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSL
AIIVSIFGLCWAPYTLLMIIRAACHGHCVPDYWYETSFWLLWANSAVNPVLYPLCHYSFR
RAFTKLLCPQKLKVQPHSSLEHCWK
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BDBM50177551 |
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n/a |
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Name | BDBM50177551 |
Synonyms: | 4-((1H-imidazol-4-yl)methyl)-N-(thiazol-2-yl)piperidine-1-carboxamide | CHEMBL377500 |
Type | Small organic molecule |
Emp. Form. | C13H17N5OS |
Mol. Mass. | 291.372 |
SMILES | O=C(Nc1nccs1)N1CCC(Cc2cnc[nH]2)CC1 |
Structure |
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