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TargetHistamine N-methyltransferase
LigandBDBM50110286
Substrate/Competitorn/a
Meas. Tech.ChEMBL_87238 (CHEMBL696458)
IC50 45±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:
BDBM50110286
n/a
NameBDBM50110286
Synonyms:(3-Piperidin-1-yl-propyl)-(1,2,3,4-tetrahydro-acridin-9-yl)-amine; Oxalic acid | CHEMBL275617
TypeSmall organic molecule
Emp. Form.C21H29N3
Mol. Mass.323.4751
SMILESC(CNc1c2CCCCc2nc2ccccc12)CN1CCCCC1
Structure
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