Inhibition of sterol Δ8 → Δ7-isomerase and Δ14-reductase by fenpropimorph tridemorph and fenpropidin in cell-free enzyme systems from Saccharomyces cerevisiae
- 1 January 1987
- journal article
- research article
- Published by Elsevier in Phytochemistry
- Vol. 26 (3) , 663-668
- https://doi.org/10.1016/s0031-9422(00)84762-7
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Chemical structure-activity relationships of the inhibition of sterol biosynthesis by N-substituted morpholines in higher plantsPesticide Biochemistry and Physiology, 1986
- Inhibition of ergosterol biosynthesis in saccharomyces cerevisiae and Ustilago maydis by tridemorph, fenpropimorph and fenpropidinPhytochemistry, 1984
- Specific effects of tridemorph on sterol biosynthesis in Ustilago maydisPesticide Biochemistry and Physiology, 1981
- 3-Phenylpropylamines, A New Class of Systemic FungicidesAngewandte Chemie International Edition in English, 1980
- Comparison of Tridemorph with Buthiobate in Antifungal Mode of ActionJournal of Pesticide Science, 1980
- Studies on Δ8–Δ7 Isomerization and Methyl Transfer of Sterols in Ergosterol Biosynthesis of Yeast1The Journal of Biochemistry, 1979
- Sterol biosynthesis from (3RS,2R)-[2-14C,2-3H]mevalonic acid in a yeast homogenate. Stereochemistry of the C-15 tritium atomJournal of the American Chemical Society, 1974
- An ab initio study of the hydration of alkylammonium groupsTheoretical Chemistry Accounts, 1973
- Studies on the Biosynthesis of Ergosterol in YeastPublished by Elsevier ,1967
- N-Substituted Tetrahydro-1,4-oxazines– A New Class of Fungicidal CompoundsAngewandte Chemie International Edition in English, 1965