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TargetHistamine N-methyltransferase
LigandBDBM50110311
Substrate/Competitorn/a
Meas. Tech.ChEMBL_87238 (CHEMBL696458)
IC50 120±n/a nM
Citation Apelt, JLigneau, XPertz, HHArrang, JMGanellin, CRSchwartz, JCSchunack, WStark, H Development of a new class of nonimidazole histamine H(3) receptor ligands with combined inhibitory histamine N-methyltransferase activity. J Med Chem45:1128-41 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Histamine N-methyltransferase
Name:Histamine N-methyltransferase
Synonyms:HNMT_RAT | Hnmt
Type:PROTEIN
Mol. Mass.:33931.03
Organism:Rattus norvegicus
Description:ChEMBL_87236
Residue:295
Sequence:
MASFMRSLFSDHSRYVESFRRFLNNSTEHQCMQEFMDKKLPGIIARIGETKAEIKILSIG
GGAGEIDLQILSKVQAQYPGICINNEVVEPNAEQIVKYKELVAKTSNMENIKFAWHKETS
SEYQKRVVEEDEEPPKWDFIHMIQMLYYVKDIPATLKFFHGLLAANAKILIILVSGTSGW
EKLWKKYGFRLPRDDLCQYVTSSDLAQILDDLGIKYECYDLLSTMDITDCFIDGNENGDL
LWDFLTETCNFIKTAPLDLKEEIMKDLQEPEFSVKKEGKVLFNNNLSFIVVEANV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50110311
n/a
NameBDBM50110311
Synonyms:CHEMBL276938 | {2-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-ethyl}-quinolin-4-yl-amine; Oxalic acid
TypeSmall organic molecule
Emp. Form.C25H31N3O
Mol. Mass.389.5331
SMILESC(COc1ccc(CCNc2ccnc3ccccc23)cc1)CN1CCCCC1
Structure
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