The physiological disposition offluvastatin, a potent inhibitor of hydroxymethylglutaryl-CoA reductase and thus cholesterol synthesis, has been studied in the mouse, rat, dog, and monkey using 14C-or 3H-labeled drug. Oral doses of fluvastatin were absorbed at a moderate to rapid rate. The extent of
Disposition of the aldose reductase inhibitor AL01576 in rats
โ Scribed by Y. H. Park; C. B. Wooldridge; J. Mattern; M. L. Stoltz; R. K. Brazzell
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 555 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0022-3549
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