Cargando…
The anti-cancer drug 5-fluorouracil is metabolized by the isolated perfused rat liver and in rats into highly toxic fluoroacetate.
We report the first demonstration of the biotransformation of the anti-cancer drug 5-fluorouracil (FU) into two new metabolites, alpha-fluoro-beta-hydroxypropionic acid (FHPA) and fluoroacetate (FAC), in the isolated perfused rat liver (IPRL) and in the rat in vivo. IPRL was perfused with solutions...
Autores principales: | Arellano, M., Malet-Martino, M., Martino, R., Gires, P. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1998
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151255/ https://www.ncbi.nlm.nih.gov/pubmed/9459149 |
Ejemplares similares
-
5-Ethynyluracil (GW776): effects on the formation of the toxic catabolites of 5-fluorouracil, fluoroacetate and fluorohydroxypropionic acid in the isolated perfused rat liver model.
por: Arellano, M., et al.
Publicado: (1997) -
Fluoroacetate in plants - a review of its distribution, toxicity to livestock and microbial detoxification
por: Leong, Lex Ee Xiang, et al.
Publicado: (2017) -
Cardiotoxicity of commercial 5-fluorouracil vials stems from the alkaline hydrolysis of this drug.
por: Lemaire, L., et al.
Publicado: (1992) -
Isolation and Identification of Sodium Fluoroacetate Degrading Bacteria from Caprine Rumen in Brazil
por: Camboim, Expedito K. A., et al.
Publicado: (2012) -
Defluorination of Sodium Fluoroacetate by Bacteria from Soil and Plants in Brazil
por: Camboim, Expedito K. A., et al.
Publicado: (2012)