Spontaneous N epsilon-methylation of L-lysine by formaldehyde.

E. Tyihák, L. Trézl, I. Rusznák

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

It has been found that the conversion of L-lysine (1) into its corresponding N epsilon-methylated derivatives, mainly N epsilon-mono-methyl-L-lysine (5; MML), but also N epsilon, N epsilon-dimethyl-L-lysine (DML) and N epsilon, N epsilon, N epsilon-trimethyl-L-lisine (TML) takes place by treatment with formaldehyde in spontaneous reaction. The identification of N epsilon-methylated lysines was carried out by different chromatographic and spectroscopic methods. This spontaneous N epsilon-methylation of L-lysine by formaldehyde may also play an important role in living organisms.

Original languageEnglish
Pages (from-to)18-20
Number of pages3
JournalPharmazie
Volume35
Issue number1
Publication statusPublished - Jan 1 1980

ASJC Scopus subject areas

  • Pharmaceutical Science

Fingerprint Dive into the research topics of 'Spontaneous N epsilon-methylation of L-lysine by formaldehyde.'. Together they form a unique fingerprint.

  • Cite this