Discovery of Perilloxazole Pseudo‐Natural Products Yields a New Sterol Biosynthesis Inhibitor Chemotype

ABSTRACT Pseudo‐natural products (PNPs) are new arrangements of natural product (NP) fragments, creating chemical spaces that extend beyond those explored by nature and are unattainable via known biosynthetic pathways. Herein, we establish the design principles for agrochemically‐active PNPs based on characteristic pesticide features. We systematically applied this strategy to discover PNP agricultural fungicides, opening up a broad new avenue for developing novel NP‐derived pesticides. We designed perilloxazole PNPs by integrating cyclohexene and isoxazoline fragments. Cheminformatics analysis demonstrates that perilloxazole PNPs combine the advantageous properties of NPs and pesticides. Biological evaluation reveals that perilloxazole represents a new chemotype of sterol biosynthesis inhibitor with low toxicity to non‐target organisms, providing a foundation for the discovery of superior green fungicides. Perilloxazole PNPs exhibit notable control efficacy against major crop diseases that cause severe agricultural losses, holding broad application prospects and high market potential.

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Publication Details

Journal
Angewandte Chemie
Published
2026-04-29
DOI
https://doi.org/10.1002/ange.5776539
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Discovery of Perilloxazole Pseudo‐Natural Products Yields a New Sterol Biosynthesis Inhibitor Chemotype

Tiantian Sun, Yanqing Gao, Hanxiao Yuan, X Q Liu et al.
Angewandte Chemie
Microbial Natural Products and Biosynthesis
article

Discovery of Perilloxazole Pseudo‐Natural Products Yields a New Sterol Biosynthesis Inhibitor Chemotype

Tiantian Sun, Yanqing Gao, Hanxiao Yuan, X Q Liu, Yuge Hu, Peng Lei, Jianqiang Miao, Xingxing Lu, Yanyan Qu
article en

Abstract

ABSTRACT Pseudo‐natural products (PNPs) are new arrangements of natural product (NP) fragments, creating chemical spaces that extend beyond those explored by nature and are unattainable via known biosynthetic pathways. Herein, we establish the design principles for agrochemically‐active PNPs based on characteristic pesticide features. We systematically applied this strategy to discover PNP agricultural fungicides, opening up a broad new avenue for developing novel NP‐derived pesticides. We designed perilloxazole PNPs by integrating cyclohexene and isoxazoline fragments. Cheminformatics analysis demonstrates that perilloxazole PNPs combine the advantageous properties of NPs and pesticides. Biological evaluation reveals that perilloxazole represents a new chemotype of sterol biosynthesis inhibitor with low toxicity to non‐target organisms, providing a foundation for the discovery of superior green fungicides. Perilloxazole PNPs exhibit notable control efficacy against major crop diseases that cause severe agricultural losses, holding broad application prospects and high market potential.

Angewandte Chemie
North West Agriculture and Forestry University (CN), Beijing Academy of Agricultural and Forestry Sciences (CN), Northwest A&F University (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 8%
Microbial Natural Products and Biosynthesis
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Discovery of Perilloxazole Pseudo‐Natural Products Yields a New Sterol Biosynthesis Inhibitor Chemotype — Tiantian Sun, Yanqing Gao, et al. · Angewandte Chemie (2026) | TGRS Research Map | TGRS