Rare benzannulated spiroketal dimers from an endophytic <i>Chaetomium</i> sp.

Three undescribed dimeric benzannulated spiroketals (1 − 3) were isolated from the fermented broth of Chaetomium sp. UJN-EF006, an endophytic fungal strain derived from Vaccinium bracteatum. Structures of these distinctive fungal products were elucidated by comprehensive spectroscopic analyses, and their absolute configurations were determined via electronic circular dichroism analyses. Of note, compounds 2 and 3 were unstable under normal storage condition, and three transformation products (3a − 3c) derived from 3 were further separated and structurally characterised. The inhibitory activities of available compounds against α-glucosidase, along with human MDA-MB-231 and A549 carcinoma cells, were also evaluated, with 3c exhibiting significant cytotoxicity.

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Publication Details

Journal
Natural Product Research
Published
2026-08-03
DOI
https://doi.org/10.1080/14786419.2026.2710817
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Rare benzannulated spiroketal dimers from an endophytic Chaetomium sp.

Hu Liu, Yinyin Wang, Jun‐Jiang Li, Hua Zhang et al.
Natural Product Research
Microbial Natural Products and Biosynthesis
article

Rare benzannulated spiroketal dimers from an endophytic Chaetomium sp.

Hu Liu, Yinyin Wang, Jun‐Jiang Li, Hua Zhang, Jun-Sheng Zhang
article en

Abstract

Three undescribed dimeric benzannulated spiroketals (1 − 3) were isolated from the fermented broth of Chaetomium sp. UJN-EF006, an endophytic fungal strain derived from Vaccinium bracteatum. Structures of these distinctive fungal products were elucidated by comprehensive spectroscopic analyses, and their absolute configurations were determined via electronic circular dichroism analyses. Of note, compounds 2 and 3 were unstable under normal storage condition, and three transformation products (3a − 3c) derived from 3 were further separated and structurally characterised. The inhibitory activities of available compounds against α-glucosidase, along with human MDA-MB-231 and A549 carcinoma cells, were also evaluated, with 3c exhibiting significant cytotoxicity.

Natural Product Research
University of Jinan (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 11%
Microbial Natural Products and Biosynthesis
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