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TargetHistamine H3 receptor
LigandBDBM50067472
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86901 (CHEMBL698411)
Ki 2.3±n/a nM
Citation Krause, MLigneau, XStark, HGarbarg, MSchwartz, JCSchunack, W 4-Alkynylphenyl imidazolylpropyl ethers as selective histamine H3-receptor antagonists with high oral central nervous system activity. J Med Chem41:4171-6 (1998) [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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50067472
n/a
NameBDBM50067472
Synonyms:4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole | 4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole (FUB 470) | CHEMBL309600
TypeSmall organic molecule
Emp. Form.C14H14N2O
Mol. Mass.226.2738
SMILESC#Cc1ccc(OCCCc2cnc[nH]2)cc1
Structure
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