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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
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设计,合成,抗真菌活性和分子对接研究新型氧化胺衍生物的新型氧化胺衍生物
Min Liu1, Wen-Rui Chen2, Xian-Song Xie2
1College of Materials and Chemical Engineering, Yibin University, A Key Lab of Process Analysis and Control of Sichuan Universities, Yibin, P. R. China.
Pest management science
|January 29, 2026
概括
新型氧胺胺表现出强烈的抗真菌活性,对抗Sclerotinia sclerotiorum. 化合物7c和7d是有效的糖酸脱酶抑制剂 (SDHI),为真菌杀菌剂耐药性提供了潜在的解决方案.
科学领域:
- 农业化学 农业化学
- 菌类学 菌类学是指菌类学.
- 药用化学 医学化学
背景情况:
- 由于滥用和过度使用,植物病原体中的真菌杀菌剂耐药性正在增加.
- 迫切需要具有广泛活性和高疗效的新型杀菌剂.
研究的目的:
- 设计和合成新型氧胺胺衍生物.
- 评估它们的抗真菌活性和作用机制.
主要方法:
- 合成了40种氧胺胺衍生物的合成.
- 在体外抗真菌测定对Sclerotinia sclerotiorum.
- 酶抑制测定向糖酸脱酶 (SDH).
- 光火和分子对接研究.
主要成果:
- 化合物7c和7d在S. sclerotiorum与fluxapyroxad.相比,在体外表现出更好的抑制作用.
- 化合物7c和7d对S. sclerotiorum和SDH的EC50和IC50值分别较低.
- 分子对接揭示了化合物7c和7d的有利结合能量.
结论:
- 化合物7c和7d是强大的糖酸脱酶抑制剂 (SDHI).
- 这些新型化合物表现出显著的抗真菌活性和克服杀真菌剂耐药性的潜力.
- 它们为农业真菌杀菌剂开发提供了有希望的前景.
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