| Literature DB >> 11081572 |
M T Paff1, D P Baccanari, S T Davis, S Cao, R L Tansik, Y M Rustum, T Spector.
Abstract
Eniluracil (5-ethynyluracil, GW 776, 776C85) is being developed as a novel modulator of 5-fluorouracil (5-FU) for the treatment of cancer. Eniluracil is an effective mechanism-based inactivator of dihydropyrimidine dehydrogenase (DPD), the first enzyme in the catabolic pathway of 5-FU. By temporarily eliminating this prevalent enzyme, eniluracil provides predictable dosing of 5-FU and enables oral administration of 5-FU to replace intravenous bolus and continuously infused dosing. New DPD is synthesized with a half-life of 2.6 days. It also eliminates the formation of problematic 5-FU catabolites. Most importantly, in laboratory animals, eniluracil increases the therapeutic index and absolute efficacy of 5-FU. Accompanying reports in this journal indicate that eniluracil has promising clinical potential.Entities:
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Year: 2000 PMID: 11081572 DOI: 10.1023/a:1006401432488
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850