Reaction Details |
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Target | Histamine H3 receptor |
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Ligand | BDBM50278449 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_501237 (CHEMBL975272) |
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Ki | 0.2±n/a nM |
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Citation | Isensee, K; Amon, M; Garlapati, A; Galaparti, A; Ligneau, X; Camelin, JC; Capet, M; Schwartz, JC; Stark, H Fluorinated non-imidazole histamine H3 receptor antagonists. Bioorg Med Chem Lett19:2172-5 (2009) [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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BDBM50278449 |
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n/a |
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Name | BDBM50278449 |
Synonyms: | 4-bromo-1-(4-(3-(piperidin-1-yl)propoxy)benzyl)piperidine | CHEMBL472466 |
Type | Small organic molecule |
Emp. Form. | C20H31BrN2O |
Mol. Mass. | 395.377 |
SMILES | BrC1CCN(Cc2ccc(OCCCN3CCCCC3)cc2)CC1 |
Structure |
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