Abstract
Investigation of Alternaria sp. AST0039, an endophytic fungus obtained from the leaf tissue of Astragalus lentiginosus, led to the isolation of (−)-(10E,15S)-4,6-dichloro-10(11)-dehydrocurvularin (1), (−)-(10E,15S)-6-chloro-10(11)-dehydrocurvularin (2), (−)-(10E,15S)-10(11)-dehydrocurvularin (3), and alterperylenepoxide A (4) together with scytalone and α-acetylorcinol. Structures of 1 and 4 were established from their spectroscopic data, and the relative configuration of 4 was determined with the help of nuclear Overhauser effect difference data. All metabolites were evaluated for their cytotoxic activity and ability to induce heat-shock and unfolded protein responses. Compounds 2 and 3 exhibited cytotoxicity to all five cancer cell lines tested and increased the level of the pro-apoptotic transcription factor CHOP, but only 3 induced the heat-shock response and caused a strong unfolded protein response.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 427-433 |
| Number of pages | 7 |
| Journal | Journal Of Natural Products |
| Volume | 80 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 24 2017 |
ASJC Scopus subject areas
- Analytical Chemistry
- Molecular Medicine
- Pharmacology
- Pharmaceutical Science
- Drug Discovery
- Complementary and alternative medicine
- Organic Chemistry
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