Microascusteroids A and B, two 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton from the marine-derived fungus Microascus sp. SCSIO 41821

Two undescribed steroids, microascusteroids A and B (1 and 2), together with four known compounds (3-6) were isolated from the marine-derived fungal strain Microascus sp. SCSIO 41821. The structures of 1 and 2 were determined by extensive spectroscopic analysis, and their absolute configurations were established by quantum chemical calculations of electronic circular dichroism (ECD) spectra. Specially, compounds 1 and 2 were unusual 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton. In addition, 1 and 2 showed medium inhibition activity against lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells and displayed mild enzyme inhibitory activity against PTP1B and cytotoxicity against human cancer cell lines H1975 and HepG2.

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Publication Details

Journal
Fitoterapia
Published
2025-04-08
DOI
https://doi.org/10.1016/j.fitote.2025.106537
Citations
1
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
1.39
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article

Microascusteroids A and B, two 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton from the marine-derived fungus Microascus sp. SCSIO 41821

Yihan Wu, Lianxiang Luo, Fei-Hua Yao, Yuqian Tang et al.
1 citations
Fitoterapia
Fungal Biology and Applications
1.39
article

Microascusteroids A and B, two 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton from the marine-derived fungus Microascus sp. SCSIO 41821

Yihan Wu, Lianxiang Luo, Fei-Hua Yao, Yuqian Tang, QI Shu-hua
article en
1 citations

Abstract

Two undescribed steroids, microascusteroids A and B (1 and 2), together with four known compounds (3-6) were isolated from the marine-derived fungal strain Microascus sp. SCSIO 41821. The structures of 1 and 2 were determined by extensive spectroscopic analysis, and their absolute configurations were established by quantum chemical calculations of electronic circular dichroism (ECD) spectra. Specially, compounds 1 and 2 were unusual 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton. In addition, 1 and 2 showed medium inhibition activity against lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells and displayed mild enzyme inhibitory activity against PTP1B and cytotoxicity against human cancer cell lines H1975 and HepG2.

FitoterapiaVol. 183
Guangdong Medical College (CN), South China Sea Institute Of Oceanology (CN)
Life below water
Openalex Percentile: Top 22%
Fungal Biology and Applications
1.39
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