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TargetPhenylethanolamine N-methyltransferase
LigandBDBM13024
Substrate/Competitorn/a
Meas. Tech.ChEMBL_303574 (CHEMBL828974)
Ki 270±n/a nM
Citation Grunewald, GLRomero, FACriscione, KR Nanomolar inhibitors of CNS epinephrine biosynthesis: (R)-(+)-3-fluoromethyl-7-(N-substituted aminosulfonyl)-1,2,3,4-tetrahydroisoquinolines as potent and highly selective inhibitors of phenylethanolamine N-methyltransferase1. J Med Chem48:1806-12 (2005) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phenylethanolamine N-methyltransferase
Name:Phenylethanolamine N-methyltransferase
Synonyms:Noradrenaline N-methyltransferase | PENT | PNMT | PNMT_HUMAN | PNMTase | Phenylethanolamine N-Methyltransferase (PNMT)
Type:Enzyme
Mol. Mass.:30852.66
Organism:Homo sapiens (Human)
Description:n/a
Residue:282
Sequence:
MSGADRSPNAGAAPDSAPGQAAVASAYQRFEPRAYLRNNYAPPRGDLCNPNGVGPWKLRC
LAQTFATGEVSGRTLIDIGSGPTVYQLLSACSHFEDITMTDFLEVNRQELGRWLQEEPGA
FNWSMYSQHACLIEGKGECWQDKERQLRARVKRVLPIDVHQPQPLGAGSPAPLPADALVS
AFCLEAVSPDLASFQRALDHITTLLRPGGHLLLIGALEESWYLAGEARLTVVPVSEEEVR
EALVRSGYKVRDLRTYIMPAHLQTGVDDVKGVFFAWAQKVGL
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  Blast E-value cutoff:
BDBM13024
n/a
NameBDBM13024
Synonyms:7-sulfonamide-THIQ 14 | CHEMBL290890 | N-(4-chlorophenyl)-3-(fluoromethyl)-1,2,3,4-tetrahydroisoquinoline-7-sulfonamide
TypeSmall organic molecule
Emp. Form.C16H16ClFN2O2S
Mol. Mass.354.827
SMILESFCC1Cc2ccc(cc2CN1)S(=O)(=O)Nc1ccc(Cl)cc1
Structure
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