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TargetHistamine H3 receptor
LigandBDBM50146126
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86904 (CHEMBL698414)
Ki 14±n/a nM
Citation Meier, GKrause, MHüls, ALigneau, XPertz, HHArrang, JMGanellin, CRSchwartz, JCSchunack, WStark, H 4-(omega-(alkyloxy)alkyl)-1H-imidazole derivatives as histamine H(3) receptor antagonists/agonists. J Med Chem47:2678-87 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histamine H3 receptor
Name:Histamine H3 receptor
Synonyms:HH3R | HRH3_RAT | Hrh3
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:48607.98
Organism:Rattus norvegicus (rat)
Description:n/a
Residue:445
Sequence:
MERAPPDGLMNASGTLAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCAS
SVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMALVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGREAG
PEPPPDAQPSPPPAPPSCWGCWPKGHGEAMPLHRYGVGEAGPGVEAGEAALGGGSGGGAA
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSL
AIIVSIFGLCWAPYTLLMIIRAACHGRCIPDYWYETSFWLLWANSAVNPVLYPLCHYSFR
RAFTKLLCPQKLKVQPHGSLEQCWK
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  Blast E-value cutoff:
BDBM50146126
n/a
NameBDBM50146126
Synonyms:1-(4-Fluoro-phenyl)-4-[3-(1H-imidazol-4-yl)-propoxy]-butan-1-one; oxalic acid | CHEMBL93376
TypeSmall organic molecule
Emp. Form.C16H19FN2O2
Mol. Mass.290.3327
SMILESFc1ccc(cc1)C(=O)CCCOCCCc1cnc[nH]1
Structure
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