نتایج جستجو برای: chlorotalonil and carboxin

تعداد نتایج: 16827185  

حسن پدرام ‌فر, , سیدعلی الهی‌ نیا, , مصطفی نیک‌ نژاد کاظم ‌پور, ,

Antagonistic fungi Trichoderma harzianum (T1, from bean fields in Ahwaz, T2, from rice fields in Rasht), T. viride (T3 from bean fields in Shahriar, T4 from the collection in Plant Pest and Disease Institute, Tehran), Gliocladium virens (from bean fields in Kamal Abad, Karaj) and some fungicides (Benomyl, Carbendazim, Carboxin-Thiram, edifenphos and Zineb) were used to control sheath blight of ...

ژورنال: علوم آب و خاک 2003
حسن پدرام ‌فر, , سیدعلی الهی‌ نیا, , مصطفی نیک‌ نژاد کاظم ‌پور, ,

Antagonistic fungi Trichoderma harzianum (T1, from bean fields in Ahwaz, T2, from rice fields in Rasht), T. viride (T3 from bean fields in Shahriar, T4 from the collection in Plant Pest and Disease Institute, Tehran), Gliocladium virens (from bean fields in Kamal Abad, Karaj) and some fungicides (Benomyl, Carbendazim, Carboxin-Thiram, edifenphos and Zineb) were used to control sheath blight of ...

2004
Stefan G.R. Wirsel Ralf T. Voegele Reto Bänninger Kurt W. Mendgen

The obligate biotrophic nature of rust fungi calls for an in planta selection scheme as a means of developing a rust transformation technology. We show that the fungicides benomyl (used as its formulated product benlate) and carboxin suppress morphogenesis of the rust fungus Uromyces fabae in vitro and disease in planta, the latter without affecting the health of the host. The limits of their a...

Journal: :Molecules 2012
Zhibing Wu Deyu Hu Jiqing Kuang Hua Cai Shixi Wu Wei Xue

A series of N-(substituted pyridinyl)-1-methyl(phenyl)-3-trifluoromethyl-1H-pyrazole-4-carboxamide derivatives were synthesized. All target compounds were characterized by spectral data (¹H-NMR, ¹³C-NMR, IR, MS) and elemental analysis and were bioassayed in vitro against three kinds of phytopathogenic fungi (Gibberella zeae, Fusarium oxysporum, Cytospora mandshurica). The results showed that so...

Journal: :The Journal of biological chemistry 1978
C J Coles T P Singer G A White G D Thorn

Carboxin (5,6-dihydro-2-methyl-l,4-oxathiin-3-carboxanilide) and a number of other carboxanilides are known to be potent inhibitors of succinate oxidation in membrane preparations from animal tissues, fungi, and bacteria, acting at the succinate dehydrogenase-coenzyme Q junction. The kinetics and the maximal extent of inhibition of succinate oxidation by carboxanilides and by thenoyltrifluoroac...

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