Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM22888 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_83644 (CHEMBL693106) |
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Ki | 84±n/a nM |
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Citation | Jablonowski, JA; Grice, CA; Chai, W; Dvorak, CA; Venable, JD; Kwok, AK; Ly, KS; Wei, J; Baker, SM; Desai, PJ; Jiang, W; Wilson, SJ; Thurmond, RL; Karlsson, L; Edwards, JP; Lovenberg, TW; Carruthers, NI The first potent and selective non-imidazole human histamine H4 receptor antagonists. J Med Chem46:3957-60 (2003) [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: | G-protein coupled receptor 97 | GPCR97 | HH3R | HISTAMINE H3 | HRH3 | HRH3_HUMAN | Histamine H3 receptor (H3) | Histamine H3L | Histamine receptor (H3 and H4) |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 48691.47 |
Organism: | Homo sapiens (Human) |
Description: | Binding assays were using CHO cells stably expressing hH3R receptors. |
Residue: | 445 |
Sequence: | MERAPPDGPLNASGALAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCTS
SAFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMLLVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGAREAA
GPEPPPEAQPSPPPPPGCWGCWQKGHGEAMPLHRYGVGEAAVGAEAGEATLGGGGGGGSV
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSFTQRFRLSRDRKVAKSL
AVIVSIFGLCWAPYTLLMIIRAACHGHCVPDYWYETSFWLLWANSAVNPVLYPLCHHSFR
RAFTKLLCPQKLKIQPHSSLEHCWK
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BDBM22888 |
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n/a |
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Name | BDBM22888 |
Synonyms: | 1-[4-(1H-imidazol-5-yl)butyl]-3-methylthiourea | Burimamide | CHEMBL12160 |
Type | Small organic molecule |
Emp. Form. | C9H16N4S |
Mol. Mass. | 212.315 |
SMILES | CNC(=S)NCCCCc1cnc[nH]1 |
Structure |
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