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TargetHistamine H3 receptor
LigandBDBM50053287
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86909 (CHEMBL698419)
Ki 313±n/a nM
Citation Ganellin, CRFkyerat, ABang-Andersen, BAthmani, STertiuk, WGarbarg, MLigneau, XSchwartz, JC A novel series of (phenoxyalkyl)imidazoles as potent H3-receptor histamine antagonists. J Med Chem39:3806-13 (1996) [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:
BDBM50053287
n/a
NameBDBM50053287
Synonyms:4-(4-Nitro-benzylsulfanylmethyl)-1H-imidazole | CHEMBL125261
TypeSmall organic molecule
Emp. Form.C11H11N3O2S
Mol. Mass.249.289
SMILES[O-][N+](=O)c1ccc(CSCc2cnc[nH]2)cc1
Structure
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