Some pyrazolo[3,4-d]pyrimidin-4(5H)-thione, pyrazolo[3,4-d][1,3]thiazin-4-one/thione, and pyrazolo[1,5-c][1,3,5]thiadiazine-4-one/thione derivatives were synthesized and screened for antifungal activity against the causal agent of rice blast disease, Magnaporthe grisea. In all cases a remarkable inhibition of fungal growth was found in the range from 10 to 200 microg mL-1. Several compounds were able to control mycelium growth at a rate of 10 microg mL-1, a concentration at which the reference compound tricyclazole was completely ineffective. At least in the case of the most active substance, at the same dose the growth of seedlings or cultured cells of rice was substantially unaffected. Results allowed definition of structural requirements either to maintain or to enhance mycotoxic activity.

Development of New Fungicides against Magnaporthe Grisea: Synthesis and Biological Activity of Pyrazolo[3,4-d][1,3]thiazine, Pyrazolo[1,5-c][1,3,5]thiadiazine and Pyrazolo[3,4-d]pyrimidine Derivatives

VICENTINI, Chiara Beatrice;FORLANI, Giuseppe;MANFRINI, Maurizio;MARES, Donatella
2002

Abstract

Some pyrazolo[3,4-d]pyrimidin-4(5H)-thione, pyrazolo[3,4-d][1,3]thiazin-4-one/thione, and pyrazolo[1,5-c][1,3,5]thiadiazine-4-one/thione derivatives were synthesized and screened for antifungal activity against the causal agent of rice blast disease, Magnaporthe grisea. In all cases a remarkable inhibition of fungal growth was found in the range from 10 to 200 microg mL-1. Several compounds were able to control mycelium growth at a rate of 10 microg mL-1, a concentration at which the reference compound tricyclazole was completely ineffective. At least in the case of the most active substance, at the same dose the growth of seedlings or cultured cells of rice was substantially unaffected. Results allowed definition of structural requirements either to maintain or to enhance mycotoxic activity.
2002
Vicentini, Chiara Beatrice; Forlani, Giuseppe; Manfrini, Maurizio; Romagnoli, C; Mares, Donatella
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1210483
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