JOURNAL 3778


Records of Natural Products
VOLUME & ISSUE
Year: 2026 Issue: 3
PAGES
p.7 - 7
STATISTICS
Viewed 13 times.
AUTHORS
  • Hao Fan
  • Xin Wang
  • Yinhan Teng
  • Pingping Wu
  • Haifang Wang
  • Yuze Li
  • Henglei Niu
  • Wei Wang
  • Xiaomei Song
  • Qing Chang
  • Dongdong Zhang
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


Guided by an integrated GNPS molecular networking strategy, the chemical investigation of endophytic fungus Aspergillus sp. FH-1 (isolated from Valeriana officinalis L.) led to the discovery of four butenolides (1-4). Their structures were elucidated through comprehensive spectroscopic data analysis, including HRESIMS, 1D/2D NMR and ECD, revealing two new congeners, asperianas A (1) and B (2), along with the known analogues 3 and 4. Notably, compounds 1 and 3 exhibited significant antifungal activity against Colletotrichum gloeosporioides, with EC50 values of 19.23 ± 1.14 and 43.36 ± 1.12 μg/mL, respectively.

KEYWORDS
  • Aspergillus sp. FH-1
  • GNPS molecular networking
  • butenolides
  • antifungal

SUPPORTING INFORMATION


Supporting Information
Download File RNP-2512-3778-SI.pdf (1.37 MB)