Reaction Details Report a problem with these data
Target
Histamine H1 receptor
Ligand
BDBM50017666
Substrate
n/a
Ki
6.06±n/a nM
Comments
PDSP_429
Citation
 Cusack, B; Nelson, A; Richelson, E Binding of antidepressants to human brain receptors: focus on newer generation compounds. Psychopharmacology (Berl) 114:559-65 (1994) [PubMed]  Article 
Target
Name:
Histamine H1 receptor
Synonyms:
H1R | HH1R | HISTAMINE H1 | HRH1 | HRH1_HUMAN
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
55808.72
Organism:
Homo sapiens (Human)
Description:
Cell pellets from SK-N-MC cells transfected with human H1 receptor were used in binding assay.
Residue:
487
Sequence:
MSLPNSSCLLEDKMCEGNKTTMASPQLMPLVVVLSTICLVTVGLNLLVLYAVRSERKLHTVGNLYIVSLSVADLIVGAVVMPMNILYLLMSKWSLGRPLCLFWLSMDYVASTASIFSVFILCIDRYRSVQQPLRYLKYRTKTRASATILGAWFLSFLWVIPILGWNHFMQQTSVRREDKCETDFYDVTWFKVMTAIINFYLPTLLMLWFYAKIYKAVRQHCQHRELINRSLPSFSEIKLRPENPKGDAKKPGKESPWEVLKRKPKDAGGGSVLKSPSQTPKEMKSPVVFSQEDDREVDKLYCFPLDIVHMQAAAEGSSRDYVAVNRSHGQLKTDEQGLNTHGASEISEDQMLGDSQSFSRTDSDTTTETAPGKGKLRSGSNTGLDYIKFTWKRLRSHSRQYVSGLHMNRERKAAKQLGFIMAAFILCWIPYFIFFMVIAFCKNCCNEHLHMFTIWLGYINSTLNPLIYPLCNENFKKTFKRILHIRS
  
Inhibitor
Name:
BDBM50017666
Synonyms:
1-(p-bromophenyl)-1-(2-pyridyl)-3-dimethylaminopropane | 2-(p-bromo-alpha-(2-dimethylaminoethyl)benzyl)pyridine | 3-(4-bromophenyl)-N,N-dimethyl-3-(2-pyridinyl)-1-propanamine | 3-(4-bromophenyl)-N,N-dimethyl-3-(pyridin-2-yl)propan-1-amine | 3-(p-bromophenyl)-3-(2-pyridyl)-N,N-dimethylpropylamine | BROMPHENIRAMINE | CHEMBL811
Type:
Small organic molecule
Emp. Form.:
C16H19BrN2
Mol. Mass.:
319.239
SMILES:
CN(C)CCC(c1ccc(Br)cc1)c1ccccn1
Structure:
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