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May 17, 2026Journal of Agricultural and Food Chemistry1 citations

S -Aryl Butenolide Thioacetates as Strigolactone Agonists: Mechanism-Guided Design for Weed Management and Crop Growth Regulation

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ZXZihao XiaCZChangheng ZhuCYChunxin Yu

Key Points

  • The study aims to develop and evaluate sulfur-containing agonists of strigolactones for their effectiveness in weed management and crop growth regulation.
  • Designed and synthesized a series of S-aryl butenolide thioacetates through a modular two-step synthetic route.
  • Evaluated biological activities using germination assays on Orobanche cumana, winter wheat tillering tests, and strawberry fruit development studies.
  • Conducted molecular docking studies with the AtD14 receptor to assess interactions.
  • Several compounds displayed significant SL-like activity, stimulating parasitic seed germination at event rates of X% (exact rates not provided) and suppressing wheat tillering (exact metrics not provided).
  • Preliminary trials indicated that specific analogues promoted strawberry fruit ripening.
  • Molecular docking results suggest suitable compatibility of arylthio substitution with the SL binding pocket, reinforcing their potential as functional SL agonists.

Abstract

Strigolactones (SLs) act as plant hormones regulating shoot architecture and as rhizospheric signals inducing parasitic weed germination. Herein, sulfur-containing SL agonists were designed and synthesized to explore their potential in weed management and crop growth regulation. A series of S-aryl butenolide thioacetates were prepared through a modular two-step synthetic route. Their biological activities were evaluated using Orobanche cumana seed germination assays, winter wheat tillering tests, and strawberry fruit development studies. Several compounds exhibited pronounced SL-like activity, including effective stimulation of parasitic seed germination or suppression of wheat tillering. Preliminary strawberry trials further indicated that certain analogues could promoted fruit ripening. Molecular docking with the AtD14 receptor suggests that arylthio substitution is compatible with the SL binding pocket and may introduce additional π–S interactions. These results identify S-aryl butenolide thioacetates as functional SL agonists and provide guidance for the development of SL-based plant growth regulators.

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Cite This Study

Xia et al. (2026) studied this question.

synapsesocial.com/papers/6a095c3f7880e6d24efe24afhttps://doi.org/10.1021/acs.jafc.5c12862
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