Two new hydroquinones bearing a 1,3-enyne moiety, pestalotioquinols G and H, together with four known compounds, including pestalotioquinol A, phomonitroester, ()-4,6,8-trihydroxy-3,4-dihydronaphthalen-1(2)-one, and scylatone were isolated from the marine fungus (BCC 35283). The structures of these compounds were elucidated by analysis of 2D-NMR and HR-MS data. The known pestalotioquinol A displayed antimalarial activity against K1 with an IC value of 19.0 μM, while pestalotioquinol G displayed weak cytotoxic activity against Vero cell lines with an IC value of 47.9 μM.
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http://dx.doi.org/10.1080/14786419.2021.1946536 | DOI Listing |
Nat Prod Res
January 2023
National Biobank of Thailand (NBT), National Science and Technology Development Agency (NSTDA), Thailand Science Park, Pathum Thani, Thailand.
Two new hydroquinones bearing a 1,3-enyne moiety, pestalotioquinols G and H, together with four known compounds, including pestalotioquinol A, phomonitroester, ()-4,6,8-trihydroxy-3,4-dihydronaphthalen-1(2)-one, and scylatone were isolated from the marine fungus (BCC 35283). The structures of these compounds were elucidated by analysis of 2D-NMR and HR-MS data. The known pestalotioquinol A displayed antimalarial activity against K1 with an IC value of 19.
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