ABSTRACT
The systemic activity of simeconazole (RS-2-(4-fluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-3-trimethylsilylpropan-2-ol) in plants was compared with those of eight other sterol demethylation inhibitor (DMI) fungicides. Simeconazole prevented the infection of Blumeria graminis (DC) Speer f sp hordei Marchal on barley leaves within a radius of several centimeters from the edge of local treatment on the leaves when the compound was separated from the leaves by glass coverslips. This reveals that simeconazole has prominent vapour-phase activity. Simeconazole showed excellent curative activity against barley powdery mildew when treated 1-3 days after inoculation. Furthermore, this indicates that simeconazole has notable translaminar activity because, when the compound was applied onto either the adaxial or abaxial leaf surface, it showed excellent efficacy against powdery mildew on the opposite side of the leaf surface of barley and cucumber. Simeconazole also showed excellent efficacy against barley powdery mildew by soil drench 24h after inoculation. This suggests that simeconazole was absorbed very quickly into the barley plant after treatment. The permeability of the compound through cuticular membranes prepared from tomato fruits was about 20% at 22 h after the treatment and was much superior to that of the other DMI fungicides tested.
Subject(s)
Fungi/drug effects , Fungicides, Industrial/toxicity , Imidazoles/toxicity , Triazoles/toxicity , Trimethylsilyl Compounds/toxicity , Cucumis sativus/microbiology , Dioxolanes/chemistry , Dioxolanes/metabolism , Dioxolanes/toxicity , Fruit/metabolism , Fruit/microbiology , Fungi/growth & development , Fungicides, Industrial/chemistry , Fungicides, Industrial/metabolism , Hordeum/microbiology , Imidazoles/chemistry , Imidazoles/metabolism , Solanum lycopersicum/microbiology , Plant Epidermis/metabolism , Plant Epidermis/microbiology , Plant Leaves/metabolism , Plant Leaves/microbiology , Plant Roots/metabolism , Plant Roots/microbiology , Soil/analysis , Triazoles/chemistry , Triazoles/metabolism , Trimethylsilyl Compounds/chemistry , Trimethylsilyl Compounds/metabolismABSTRACT
The systemic activity of simeconazole (RS-2-(4-fluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-3-trimethylsilylpropan-2-ol) and a number of its derivatives in plants has been investigated to establish which portion of the structure of the molecule contributes to this outstanding activity. The results revealed that the hydroxyl group of the simeconazole moiety is essential for vapour-phase activity and translocation from roots of the compound. They showed that the presence of a fluorine atom in the structure was not indispensable for vapour-phase activity or translocation from roots, although the fluorine atom contributed to these systemic movements. In addition, it was found that the fungicidal activity of simeconazole against Rhizoctonia solani Kühn and Blumeria graminis DC fsp hordei Marchal is potentiated by the fluorine atom, since the activity of a compound which lacked fluorine in the 4-position of the phenyl ring was inferior to that of simeconazole. A compound in which the silicon atom of simeconazole was replaced by a carbon atom showed lower antifungal activity than simeconazole, while phytotoxicity was caused in rice plants by soil drench of the compound. Therefore, the silicon atom of simeconazole may contribute to its selectivity between fungi and plants.
