Target
Histamine N-methyltransferase
Ligand
BDBM50110300
Substrate
n/a
Meas. Tech.
ChEMBL_87238 (CHEMBL696458)
IC50
48±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 Chem 45:1128-41 (2002) [PubMed]  Article 
Target
Name:
Histamine N-methyltransferase
Synonyms:
HNMT_RAT | Hnmt
Type:
PROTEIN
Mol. Mass.:
33931.03
Organism:
Rattus norvegicus
Description:
ChEMBL_87236
Residue:
295
Sequence:
MASFMRSLFSDHSRYVESFRRFLNNSTEHQCMQEFMDKKLPGIIARIGETKAEIKILSIGGGAGEIDLQILSKVQAQYPGICINNEVVEPNAEQIVKYKELVAKTSNMENIKFAWHKETSSEYQKRVVEEDEEPPKWDFIHMIQMLYYVKDIPATLKFFHGLLAANAKILIILVSGTSGWEKLWKKYGFRLPRDDLCQYVTSSDLAQILDDLGIKYECYDLLSTMDITDCFIDGNENGDLLWDFLTETCNFIKTAPLDLKEEIMKDLQEPEFSVKKEGKVLFNNNLSFIVVEANV
  
Inhibitor
Name:
BDBM50110300
Synonyms:
CHEMBL15056 | N-(4-(3-(piperidin-1-yl)propoxy)phenethyl)-5,6,7,8-tetrahydroacridin-9-amine | {2-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-ethyl}-(1,2,3,4-tetrahydro-acridin-9-yl)-amine; Oxalic acid
Type:
Small organic molecule
Emp. Form.:
C29H37N3O
Mol. Mass.:
443.6236
SMILES:
C(COc1ccc(CCNc2c3CCCCc3nc3ccccc23)cc1)CN1CCCCC1
Structure:
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