| Literature DB >> 28139929 |
Bharat P Bashyal1, E M Kithsiri Wijeratne1, Joseph Tillotson2, A Elizabeth Arnold3, Eli Chapman2, A A Leslie Gunatilaka1.
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.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28139929 PMCID: PMC5504521 DOI: 10.1021/acs.jnatprod.6b00960
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050