Ergostane steroids from <i>Aspergillus</i> sp. M904 in Vietnam

Seven ergostane steroids were isolated from the cultures of Aspergillus sp. M904, an endophytic fungus isolated from the marine sediment sample collected at a depth of ten meters in Binh Dinh, Vietnam. These compounds include 5α,6α-epoxy-(22E,24R)-ergosta-8(14),22-diene-3β,7α-diol (1), 5α,6α-epoxy-(22E,24R)-ergosta-8(9),22-diene-3β,7α-diol (2), ergosterol (3), ergosterol peroxide (4), 3β,5α,6α-trihydroxy-ergosta-7,22-diene (5), 3β,5α,9α-trihydroxy-ergosta-7,22-diene-6-one (6), 3β-hydroxy-5α,9α-epoxy-ergosta-7,22-dien-6-one (7). Their structures were identified through MS and NMR data analyses. All compounds were evaluated for their antimicrobial activity against a panel of clinically significant microorganisms. Compounds 1–7 had inhibitory activity against from one to six tested strains with MIC values from 64–256 µg/mL.

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Publication Details

Journal
Vietnam Journal of Marine Science and Technology
Published
2024-12-10
DOI
https://doi.org/10.15625/1859-3097/22128
Primary Topic
Phytochemical Studies and Bioactivities
Type
article
Field-Weighted Citation Impact
0.00

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article

Ergostane steroids from Aspergillus sp. M904 in Vietnam

Van Cuong Pham, Thi Thanh Van Trinh, Van Nam Vu, Đoàn Thị Mai Hương et al.
Vietnam Journal of Marine Science and Technology
Phytochemical Studies and Bioactivities
article

Ergostane steroids from Aspergillus sp. M904 in Vietnam

Van Cuong Pham, Thi Thanh Van Trinh, Van Nam Vu, Đoàn Thị Mai Hương, Mai Ánh Nguyễn, Thùy Linh Nguyễn, Thi Hong Minh Le, Brian Murphy
article en

Abstract

Seven ergostane steroids were isolated from the cultures of Aspergillus sp. M904, an endophytic fungus isolated from the marine sediment sample collected at a depth of ten meters in Binh Dinh, Vietnam. These compounds include 5α,6α-epoxy-(22E,24R)-ergosta-8(14),22-diene-3β,7α-diol (1), 5α,6α-epoxy-(22E,24R)-ergosta-8(9),22-diene-3β,7α-diol (2), ergosterol (3), ergosterol peroxide (4), 3β,5α,6α-trihydroxy-ergosta-7,22-diene (5), 3β,5α,9α-trihydroxy-ergosta-7,22-diene-6-one (6), 3β-hydroxy-5α,9α-epoxy-ergosta-7,22-dien-6-one (7). Their structures were identified through MS and NMR data analyses. All compounds were evaluated for their antimicrobial activity against a panel of clinically significant microorganisms. Compounds 1–7 had inhibitory activity against from one to six tested strains with MIC values from 64–256 µg/mL.

Vietnam Journal of Marine Science and TechnologyVol. 24(4)
University of Illinois Chicago (US), Institute of Marine Geology and Geophysics (VN), Vietnam Academy of Science and Technology (VN)
National Institutes of Health, Fogarty International Center
Openalex Percentile: Top 79%
Phytochemical Studies and Bioactivities
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