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TargetPhenylethanolamine N-methyltransferase
LigandBDBM13023
Substrate/Competitorn/a
Meas. Tech.ChEMBL_152393 (CHEMBL765516)
Ki 340±n/a nM
Citation Grunewald, GLDahanukar, VHTeoh, BCriscione, KR 3,7-Disubstituted-1,2,3,4-tetrahydroisoquinolines display remarkable potency and selectivity as inhibitors of phenylethanolamine N-methyltransferase versus the alpha2-adrenoceptor. J Med Chem42:1982-90 (1999) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phenylethanolamine N-methyltransferase
Name:Phenylethanolamine N-methyltransferase
Synonyms:Noradrenaline N-methyltransferase | PNMT | PNMT_BOVIN | PNMTase
Type:Enzyme
Mol. Mass.:30916.97
Organism:Bos taurus (bovine)
Description:n/a
Residue:283
Sequence:
MSGTDRSQAAGAVPDSDPGLAAVSSAYQRFEPRAYLRNNYAPPRGDLSCPDGVGPWKLRC
LAQTFATGEVSGRTLIDIGSGPTIYQLLSACAHFEDITMTDFLEVNRQELRLWLREEPGA
FDWSVYSQHVCLIEGKGESWQEKECQLRARVKRILPIDVHRPQPLGAGGLAPLPADALVS
AFCLEAVSPDLASFQRALDHITTLLRPGGHLLLIGALEESWYLAGEARLAVVPVREEEVR
EALVRTATRCGICARTPMPAHLQTGVDDVKGIFFTRAQKKVGV
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  Blast E-value cutoff:
BDBM13023
n/a
NameBDBM13023
Synonyms:3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-7-sulfonamide | 7-sulfonamide-THIQ 13 | CHEMBL41647
TypeSmall organic molecule
Emp. Form.C10H14N2O3S
Mol. Mass.242.295
SMILESNS(=O)(=O)c1ccc2CC(CO)NCc2c1
Structure
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