Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50365053 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_804715 (CHEMBL1953342) |
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Ki | 10±n/a nM |
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Citation | Sundar, BG; Bailey, TR; Dunn, D; Hostetler, GA; Chatterjee, S; Bacon, ER; Yue, C; Schweizer, D; Aimone, LD; Gruner, JA; Lyons, J; Raddatz, R; Lesur, B Novel morpholine ketone analogs as potent histamine H3 receptor inverse agonists with wake activity. Bioorg Med Chem Lett22:1546-9 (2012) [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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BDBM50365053 |
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n/a |
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Name | BDBM50365053 |
Synonyms: | CHEMBL1951062 |
Type | Small organic molecule |
Emp. Form. | C22H34N2O3 |
Mol. Mass. | 374.517 |
SMILES | C[C@@H]1CCCN1CCCOc1ccc(cc1)C(=O)CN1C[C@H](C)O[C@H](C)C1 |r| |
Structure |
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