1. Academic Validation
  2. Natural Alkaloid Waltherione F-Derived Hydrazide Compounds Evaluated in an Agricultural Fungicidal Field

Natural Alkaloid Waltherione F-Derived Hydrazide Compounds Evaluated in an Agricultural Fungicidal Field

  • J Agric Food Chem. 2023 Aug 16;71(32):12333-12345. doi: 10.1021/acs.jafc.3c03937.
Zhanfang Chen 1 Hongbin Fang 1 Jing Chang 1 Tiancheng Zhang 1 Yanhong Cui 2 Lingxiao Zhang 1 Junkang Sui 1 Qingping Ma 1 Peisen Su 1 Juyuan Wang 1 Jing Ru 3 Yucheng Gu 4 Hengjia Zhang 1 Xuewen Hua 1
Affiliations

Affiliations

  • 1 College of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, P. R. China.
  • 2 College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310014, P. R. China.
  • 3 College of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252000, P. R. China.
  • 4 Jealott's Hill International Research Centre, Syngenta Ltd., Bracknell RG42 6EY, U.K.
Abstract

In this project, quinoline and quinolone-containing hydrazide compounds were designed and synthesized by introducing a bioactive hydrazide group into the skeleton of waltherione F. The fungicidal activity revealed that some hydrazide compounds exhibited excellent and broad-spectrum fungicidal activity; especially, compounds E8, E12, and E16 showed more than 90% or even 100% inhibition rates against most pathogens at 50 μg·mL-1. The fungicidal mechanism indicated that compound E8 may affect the normal function of the plasma membrane, further generating changes in the morphology and subcellular structure of mycelia. Simultaneously, Fusarium graminearum may resist the E8-treated stress through the metabolic pathways related to l-glutamate, l-glutamine, and glutathione. Finally, the effect of compound E8 on wheat seedling's growth and the toxicity to zebrafish were accomplished. These results will provide important guidance to discover novel fungicidal lead compounds and explore new targets, which are effective ways to alleviate the increasingly severe drug resistance.

Keywords

fungicidal activity; hydrazide; mechanism of action; structural optimization; structure−activity relationship.

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