Discovery of Imidazo[1, 2- <i>a</i> ]pyridine Hydrazone Derivatives as Novel Antifungal Tubulin-Targeting Agents via a Scaffold-Hopping Strategy

formed multiple hydrogen bonds and π-π interactions with tubulin, and further induced intracellular microtubule aggregation, thereby disrupting both hyphal morphology and cellular architecture. This study provides strong evidence for structural diversification in tubulin-targeting antifungal agents, offering new perspectives for overcoming existing limitations in antifungal therapy.

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Publication Details

Journal
Journal of Agricultural and Food Chemistry
Published
2026-05-29
DOI
https://doi.org/10.1021/acs.jafc.5c12629
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Discovery of Imidazo[1, 2- a ]pyridine Hydrazone Derivatives as Novel Antifungal Tubulin-Targeting Agents via a Scaffold-Hopping Strategy

Zhou‐Qing Long, Xian-Qun Hu, Long‐Fei Li, L Y Zhang et al.
Journal of Agricultural and Food Chemistry
Synthesis and biological activity
article

Discovery of Imidazo[1, 2- a ]pyridine Hydrazone Derivatives as Novel Antifungal Tubulin-Targeting Agents via a Scaffold-Hopping Strategy

Zhou‐Qing Long, Xian-Qun Hu, Long‐Fei Li, L Y Zhang, Xiang Zhou, Hong‐Wu Liu, Zhenhua Li, Yuanyuan Wu, Yu Long, Xin-Ming Yang, Mei Li, Song Yang
article en

Abstract

formed multiple hydrogen bonds and π-π interactions with tubulin, and further induced intracellular microtubule aggregation, thereby disrupting both hyphal morphology and cellular architecture. This study provides strong evidence for structural diversification in tubulin-targeting antifungal agents, offering new perspectives for overcoming existing limitations in antifungal therapy.

Journal of Agricultural and Food Chemistry
Bureau of Plant Industry (PH), Guizhou University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Zero hunger
Openalex Percentile: Top 10%
Synthesis and biological activity
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