Oxidation of guanine Nucleosides to 4-amidinocarbamoyl-5-hydroxyimidazoles by dimethyldioxirane

R.J.H. Davies, C. Stevenson, S. Kumar, J. Lyle, L. Cosby, John Malone, Derek Boyd, Narain Sharma, A.P. Hunter, B.K. Stein

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Final oxidation products generated from guanosine and 2'-deoxyguano sine by reaction with dimethyldioxirane have been identified as 4-amidinocarbamoyl-5-hydroxyimidazoles.
Original languageEnglish
Pages (from-to)1355-1357
Number of pages3
JournalNucleosides Nucleotides & Nucleic Acids
Volume22
Issue number5-8
DOIs
Publication statusPublished - 2003

ASJC Scopus subject areas

  • Biochemistry
  • Genetics

Fingerprint

Dive into the research topics of 'Oxidation of guanine Nucleosides to 4-amidinocarbamoyl-5-hydroxyimidazoles by dimethyldioxirane'. Together they form a unique fingerprint.

Cite this