Cytochalasinols A and B, Two New Cytochalasins From the Fungus <i>Xylaria necrophora</i> SZSS1‐2‐2

Two new cytochalasins (1 and 2) were isolated from the fermentation products of the fungus Xylaria necrophora SZSS1-2-2, along with nine known compounds: compound 3, arbuschalasin B (4), cytochalasin C (5), cytochalasin D (6), 19,20-epoxycytochalasin C (7), 19,20-epoxycytochalasin D (8), cytochalasin R (9), cytochalasin D 13,14-epoxide (10), and arbuschalasin A (11). The structures and absolute configurations of these compounds were elucidated by spectroscopic analyses, electronic circular dichroism, and GIAO <sup>13</sup>C NMR computational methods. All isolated compounds were evaluated for their biological activities, and the results indicated that compounds 5-10 exhibited notable cytotoxic effects against the tested cell lines. However, none of the compounds showed antibacterial activity.

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Journal
Chemistry & Biodiversity
Published
2025-11-25
DOI
https://doi.org/10.1002/cbdv.202503213
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Cytochalasinols A and B, Two New Cytochalasins From the Fungus Xylaria necrophora SZSS1‐2‐2

Yang Yu, Chen Sun, Er‐Wei Li, Shuai‐Ming Zhu et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

Cytochalasinols A and B, Two New Cytochalasins From the Fungus Xylaria necrophora SZSS1‐2‐2

Yang Yu, Chen Sun, Er‐Wei Li, Shuai‐Ming Zhu, You‐Zhi Zhang, Yang Yi, Chang‐Wei Li, Yang Zhang, Lixia Chen, Xue Zhao, Qian Luo, Rui Xu
article en

Abstract

Two new cytochalasins (1 and 2) were isolated from the fermentation products of the fungus Xylaria necrophora SZSS1-2-2, along with nine known compounds: compound 3, arbuschalasin B (4), cytochalasin C (5), cytochalasin D (6), 19,20-epoxycytochalasin C (7), 19,20-epoxycytochalasin D (8), cytochalasin R (9), cytochalasin D 13,14-epoxide (10), and arbuschalasin A (11). The structures and absolute configurations of these compounds were elucidated by spectroscopic analyses, electronic circular dichroism, and GIAO <sup>13</sup>C NMR computational methods. All isolated compounds were evaluated for their biological activities, and the results indicated that compounds 5-10 exhibited notable cytotoxic effects against the tested cell lines. However, none of the compounds showed antibacterial activity.

Chemistry & BiodiversityVol. 23(2)
Shenyang Pharmaceutical University (CN), Chinese Academy of Sciences (CN), Academy of Military Medical Sciences (CN), Institute of Microbiology (CN)
Openalex Percentile: Top 60%
Microbial Natural Products and Biosynthesis
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Cytochalasinols A and B, Two New Cytochalasins From the Fungus <i>Xylaria necrophora</i> SZSS1‐2‐2 — Yang Yu, Chen Sun, et al. · Chemistry & Biodiversity (2025) | TGRS Research Map | TGRS