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A Novel Phenamacril Derivative Targeting Myosin I for the Control of Gray Mold Caused by Botrytis cinerea

  • Songtao Liu
  • , Fei Liu
  • , Xiyuan Zhu
  • , Ziyang Yang
  • , Wanting Zhang
  • , Fangying Jia
  • , Xinyan Chu
  • , Renkai Lei
  • , Linwei Li
  • , Shu Xu
  • , Wei Song
  • , Jiaxing Yan
  • , Jingjing Guo
  • , Yu Chen
  • , Xu Feng
  • , Feng Zhang
  • CAS - Jiangsu Institute of Botany
  • Nanjing Agricultural University

Research output: Contribution to journal › Article › peer-review

Abstract

Gray mold caused by Botrytis cinerea severely impacts global crop productivity. In this study, we identified B33 [(Z)-3-amino-N-(3-chloro-4-fluorobenzyl)-2-cyano-3-phenylacrylamide], a novel phenamacril derivative bearing a distinctive substitution pattern where the ester group is replaced by an amino group. As an unprecedented small-molecule inhibitor targeting B. cinerea myosin I (BcMyoI), it represents an unexplored antifungal mode of action for gray mold disease management. Combined assays including phenotypic screening, ATPase inhibition, and microscale thermophoresis (MST) confirmed that B33 binds BcMyoI, and molecular dynamics simulations revealed stable interactions with the conserved phenamacril-binding pocket. In the greenhouse experiment, the protective effect of B33 on strawberry leaves was comparable to that of the commercial fungicide boscalid.

Original languageEnglish
Pages (from-to)26144-26154
Number of pages11
JournalJournal of agricultural and food chemistry
Volume74
Issue number33
DOIs
Publication statusPublished - 26 Aug 2026

Keywords

  • Antifungal agent
  • Botrytis cinerea
  • Myosin I inhibitor
  • Phenamacril

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