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Journal ArticleDOI

Comparaisons des modes d'action fongitoxique du Triadiméfon (Meb 6447), du Triarimol et de la Triforine

P. Leroux, +1 more
- 01 Jul 1976 - 
- Vol. 86, Iss: 3, pp 276-279
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This article is published in Journal of Phytopathology.The article was published on 1976-07-01. It has received 12 citations till now.

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Citations
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A mutant of Ustilago maydis deficient in sterol C-14 demethylation: Characteristics and sensitivity to inhibitors of ergosterol biosynthesis☆

TL;DR: Findings support the contention that inhibition of sterol C-14 demethylation in U. maydis is the primary mode of toxicity of fenarimol, etaconazole, and miconazole.
Journal ArticleDOI

Mechanism of resistance to fenarimolin Aspergillus nidulans

TL;DR: Resistance might be correlated with increased excretion of fungal metabolites, which in turn may be related with reduced fitness of fenarimol-resistant mutants.
References
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Journal ArticleDOI

Specific effects of triarimol on sterol biosynthesis in Ustilago maydis

TL;DR: This study indicates that in U. maydis triarimol inhibits three reactions in ergosterol biosynthesis, all of which involve the D ring and the side chain of the sterol molecule: demethylation at C-14; introduction of the C-22(23) double bond; and reduction of theC-24(28) double Bond.
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Effect of the antibiotic, cycloheximide, on the metabolism and growth of saccharomyces pastorianus

TL;DR: A block of glutamine synthesis by cycloheximide may be sufficient to account for the toxicity of the antibiotic, but the failure of exogenous sources of glutamines to reverse the toxicity indicates that other reactions in cell metabolism may be as sensitive to cyclo heximide as the synthesis of glutamate.
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Similarities between the systemic fungicides triforine and triarimol

TL;DR: The various similarities between triforine and triarimol suggest a common mode of action for the two compounds, which are structurally unrelated but have similar antifungal spectrum.
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Lipid Synthesis in the Presence of Nitrogenous Compounds in Chlorella pyrenoidosa

TL;DR: The incorporation of Chlorella pyrenoidosa into nonvolatile water-soluble compounds (amino acids, organic acids and carbohydrates) with pH optimum between 4 and 5.5 was reported in this article.
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Laboratory and greenhouse evaluation of a new systemic fungicide, N,N'-bis-(1-formamido-2,2,2-trichloroethyl)- piperazine (CELA W 524)

TL;DR: The new systemic fungicide CELA W 524 was shown to display a moderate to distinct fungitoxic activity in vitro towards several pathogenic and non-pathogenic fungi, which proved to be either rather phytotoxic or virtually non-phytotoxic depending on the inert ingredients present.