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 language | English |
|---|---|
| Pages (from-to) | 357-369 |
| Number of pages | 13 |
| Journal | Nucleosides, Nucleotides and Nucleic Acids |
| Volume | 19 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - 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
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver