Mannosylxylarinols A and B, Two New 3,4‐ Seco ‐ergostane‐type Steroidal Saponins From the Fungus Xylaria necrophora SZSS1‐2‐2

ABSTRACT Two new 3,4‐ seco ‐ergostane‐type steroidal saponins ( 1 and 2 ) were isolated from the fermentation products of the fungus Xylaria necrophora SZSS1‐2‐2, together with four known compounds: 2‐hexylidene‐3‐methylsuccinic acid ( 3 ), xylcarpin C ( 4 ), (24 R )‐22,23‐dihydroxy‐ergosta‐4,6,8(14)‐trien‐3‐one 23‐ β ‐D‐glucopyranoside ( 5 ), and 5‐carboxymellein ( 6 ). The structures and absolute configurations of the new compounds were elucidated by comprehensive spectroscopic analyses, electronic circular dichroism (ECD), and GIAO 1 3 C NMR computational methods, and chemical hydrolysis followed by derivatization to determine the D‑mannose configuration of the sugar moiety. All isolated compounds ( 1–6 ) were evaluated for their biological activities. Only compound 5 showed selective inhibitory activity, inhibiting BV2 microglial cells with an IC 50 value of 17.10 ± 4.18 µM. Additionally, none of the compounds exhibited antimicrobial activity against the tested microorganisms.

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Journal
Chemistry & Biodiversity
Published
2026-09-30
DOI
https://doi.org/10.1002/cbdv.71800
Primary Topic
Microbial Natural Products and Biosynthesis
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article
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Mannosylxylarinols A and B, Two New 3,4‐ Seco ‐ergostane‐type Steroidal Saponins From the Fungus Xylaria necrophora SZSS1‐2‐2

Erwei Li, You‐Zhi Zhang, Chang‐Wei Li, Yu Yang et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

Mannosylxylarinols A and B, Two New 3,4‐ Seco ‐ergostane‐type Steroidal Saponins From the Fungus Xylaria necrophora SZSS1‐2‐2

Erwei Li, You‐Zhi Zhang, Chang‐Wei Li, Yu Yang, Lixia Chen, Xue Zhao, Rui Xu, Qian Luo, Yu‐Ying Wei, Hui‐Fang Tan
article en

Abstract

ABSTRACT Two new 3,4‐ seco ‐ergostane‐type steroidal saponins ( 1 and 2 ) were isolated from the fermentation products of the fungus Xylaria necrophora SZSS1‐2‐2, together with four known compounds: 2‐hexylidene‐3‐methylsuccinic acid ( 3 ), xylcarpin C ( 4 ), (24 R )‐22,23‐dihydroxy‐ergosta‐4,6,8(14)‐trien‐3‐one 23‐ β ‐D‐glucopyranoside ( 5 ), and 5‐carboxymellein ( 6 ). The structures and absolute configurations of the new compounds were elucidated by comprehensive spectroscopic analyses, electronic circular dichroism (ECD), and GIAO 1 3 C NMR computational methods, and chemical hydrolysis followed by derivatization to determine the D‑mannose configuration of the sugar moiety. All isolated compounds ( 1–6 ) were evaluated for their biological activities. Only compound 5 showed selective inhibitory activity, inhibiting BV2 microglial cells with an IC 50 value of 17.10 ± 4.18 µM. Additionally, none of the compounds exhibited antimicrobial activity against the tested microorganisms.

Chemistry & BiodiversityVol. 23(10)
Shenyang Pharmaceutical University (CN), Chinese Academy of Sciences (CN), Academy of Military Medical Sciences (CN), Institute of Microbiology (CN)
Openalex Percentile: Top 13%
Microbial Natural Products and Biosynthesis
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Mannosylxylarinols A and B, Two New 3,4‐ Seco ‐ergostane‐type Steroidal Saponins From the Fungus Xylaria necrophora SZSS1‐2‐2 — Erwei Li, You‐Zhi Zhang, et al. · Chemistry & Biodiversity (2026) | TGRS Research Map | TGRS