Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50127847 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_788422 (CHEMBL1918187) |
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Ki | 40±n/a nM |
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Citation | Singh, GS; Mmatli, EE Recent progress in synthesis and bioactivity studies of indolizines. Eur J Med Chem46:5237-57 (2011) [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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BDBM50127847 |
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n/a |
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Name | BDBM50127847 |
Synonyms: | 1-Phenyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-indolizine | CHEMBL299075 |
Type | Small organic molecule |
Emp. Form. | C28H30N2O |
Mol. Mass. | 410.5506 |
SMILES | C(COc1ccc(cc1)-c1cn2ccccc2c1-c1ccccc1)CN1CCCCC1 |
Structure |
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