Stereoselectivity of paclobutrazol enantiomers to oxidative stress in wheat

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL Chirality Pub Date : 2024-01-17 DOI:10.1002/chir.23638
Chao Yang, Hao Li, Huajun Liang, Bo Huang, Yitao Sun, Wenlong Yang, Yilun Wu, Youhe Cui, Jiangbo Hai, Zhoujia Dong
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Abstract

Chiral pesticides have the special chiral structures, so enantioselective biological effects are usually observed in living organisms. Current study used paclobutrazol as a case study and explored the enantioselective degradation and oxidative stress effect on wheat. The results demonstrated that the degradation of R-paclobutrazol was faster than S-paclobutrazol significantly and improved the content of MDA and O2 in wheat plants, which proved that the R-paclobutrazol induced oxidative damage in wheat, showing selective biological effects, and S-paclobutrazol was friendly to wheat. This study provided a theoretical basis for the selective activity of chiral pesticides and the development of chiral pesticide monomers.

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小麦中对映体对氧化应激的立体选择性
手性农药具有特殊的手性结构,因此通常会在生物体内观察到对映体选择性生物效应。本研究以百草枯为例,探讨了其对映体选择性降解及对小麦的氧化胁迫效应。结果表明,R-paclobutrazol的降解速度明显快于S-paclobutrazol,并提高了小麦植株体内MDA和O2-的含量,证明R-paclobutrazol诱导小麦氧化损伤,表现出选择性生物效应,而S-paclobutrazol对小麦友好。该研究为手性农药的选择性活性和手性农药单体的开发提供了理论依据。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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