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TargetHistamine H3 receptor
LigandBDBM50092866
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86763 (CHEMBL698663)
Ki 91±n/a nM
Citation Stark, HSadek, BKrause, MHüls, ALigneau, XGanellin, CRArrang, JMSchwartz, JCSchunack, W Novel histamine H(3)-receptor antagonists with carbonyl-substituted 4-(3-(phenoxy)propyl)-1H-imidazole structures like ciproxifan and related compounds. J Med Chem43:3987-94 (2000) [PubMed]
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50092866
n/a
NameBDBM50092866
Synonyms:4-{4-[3-(1H-Imidazol-4-yl)-propoxy]-phenyl}-butan-2-one; compound with but-2-enedioic acid(0.5M H2O) | CHEMBL265106
TypeSmall organic molecule
Emp. Form.C16H20N2O2
Mol. Mass.272.3422
SMILESCC(=O)CCc1ccc(OCCCc2cnc[nH]2)cc1
Structure
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