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Detection of <Emphasis Type="Italic">N</Emphasis>-monomethyl-lysine generated by metabolic transmethylation
Authors:Email author" target="_blank">Huba?KalászEmail author  Imre?Klebovich  Katalin?Balogh-Nemes  ágnes?Szilágyi  Mária?Tihanyi  Tibor?Szarvas  József?Lengyel
Institution:(1) Department of Pharmacology and Pharmacotherapy, Semmelweis University, 1089 Budapest, Nagyvárad tér 4, Hungary;(2) EGIS Pharmaceutical Works, Budapest, Hungary;(3) Department of Pharmaceutics, Semmelweis University, Budapest, Hungary;(4) Institute of Isotopes Co. Ltd., Budapest, Hungary;(5) Central Isotope Laboratory, Semmelweis University, Budapest, Hungary;(6) Department of Pharmacology & Therapeutics, Faculty of Medicine & Health Sciences, United Arab Emirates University, P.O.Box 17666, Al Ain, United Arab Emirates
Abstract:Administration of radiolabelled deprenyl to rats resulted in the urinary elimination of a 14C-labelled Nepsi-monomethyl-lysine. An increased level of Nepsi-monomethyl-lysine was found following an oral dose of another drug, also containing an N-methyl group. The urine sample was treated with 9-fluorenylmethoxycarbonyl chloride and then subjected to high-performance liquid chromatography (HPLC); the radioactive fraction was identified as Nepsi-monomethyl-lysine by using HPLC-MS in electrospray mode. Identification of Nepsi-monomethyl-lysine in the radioactive fraction gives experimental proof of transmethylation from a well-known drug to an endogenous compound.
Keywords:HPLC  HPLC/MS/MS  Methylation  N-Monomethyl-lysine  Deprenyl  Urinary
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