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TargetHistamine H2 receptor
LigandBDBM22542
Substrate/Competitorn/a
Meas. Tech.ChEMBL_643317 (CHEMBL1177488)
Ki>1000±n/a nM
Citation Ishikawa, MFuruuchi, TYamauchi, MYokoyama, FKakui, NSato, Y Synthesis and structure-activity relationships of N-aryl-piperidine derivatives as potent (partial) agonists for human histamine H3 receptor. Bioorg Med Chem18:5441-8 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histamine H2 receptor
Name:Histamine H2 receptor
Synonyms:Gastric receptor I | H2R | HISTAMINE H2 | HRH2 | HRH2_HUMAN | Histamine H2 receptor | Histamine H2-Gs alpha S
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:40115.31
Organism:Homo sapiens (Human)
Description:n/a
Residue:359
Sequence:
MAPNGTASSFCLDSTACKITITVVLAVLILITVAGNVVVCLAVGLNRRLRNLTNCFIVSL
AITDLLLGLLVLPFSAIYQLSCKWSFGKVFCNIYTSLDVMLCTASILNLFMISLDRYCAV
MDPLRYPVLVTPVRVAISLVLIWVISITLSFLSIHLGWNSRNETSKGNHTTSKCKVQVNE
VYGLVDGLVTFYLPLLIMCITYYRIFKVARDQAKRINHISSWKAATIREHKATVTLAAVM
GAFIICWFPYFTAFVYRGLRGDDAINEVLEAIVLWLGYANSALNPILYAALNRDFRTGYQ
QLFCCRLANRNSHKTSLRSNASQLSRTQSREPRQQEEKPLKLQVWSGTEVTAPQGATDR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM22542
n/a
NameBDBM22542
Synonyms:4-(1H-imidazol-4-ylmethyl)piperidine | 4-(1H-imidazol-5-ylmethyl)piperidine | Immepip
TypeSmall organic molecule
Emp. Form.C9H15N3
Mol. Mass.165.2355
SMILESC(C1CCNCC1)c1cnc[nH]1
Structure
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