Skip to main navigation Skip to search Skip to main content

Rational design of selective antimetabolites of DNA-thymine biosynthesis: 5-propynylpyrimidine nucleoside derivatives

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

A novel series of 5-propynylpyrimidine nucleosides are proposed as potential antimetabolites of DNA-thymine biosynthesis. This proposal is based on the results of detailed mechanistic analyses of the molecular interactions between dTMP synthase and its inhibitors. It is proposed that a propynyl side-chain at the 5-position of dUMP, bearing an appropriate leaving group, would cause irreversible inactivation of dTMP synthase, which would not require the presence of the cofactor, CH2H4folate.

Original languageEnglish
Pages (from-to)357-369
Number of pages13
JournalNucleosides, Nucleotides and Nucleic Acids
Volume19
Issue number1-2
DOIs
StatePublished - 2000

Fingerprint

Dive into the research topics of 'Rational design of selective antimetabolites of DNA-thymine biosynthesis: 5-propynylpyrimidine nucleoside derivatives'. Together they form a unique fingerprint.

Cite this