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Published on: February 9, 2021
Cytotoxic Prenylated Stilbenes Isolated from Macaranga tanarius
Tiphaine Péresse1, Gwenaëlle Jézéquel1, Pierre-Marie Allard2
1Institut de Chimie des Substances Naturelles, CNRS, ICSN UPR2301, University of Paris-Saclay , 91198, Gif-sur-Yvette, France.
Researchers discovered seven new prenylated stilbenes from Macaranga tanarius fruits. These compounds, part of the schweinfurthin series, were tested for cytotoxic activity against glioblastoma and lung cancer cells.
Area of Science:
- Natural Product Chemistry
- Phytochemistry
- Medicinal Chemistry
Background:
- Macaranga species are a rich source of bioactive compounds.
- Prenylated stilbenes exhibit diverse biological activities, including cytotoxicity.
- The schweinfurthin series is of interest for potential anticancer agents.
Purpose of the Study:
- To discover novel cytotoxic prenylated stilbenes from Macaranga tanarius.
- To investigate the chemical constituents of Macaranga tanarius fruits.
- To evaluate the anticancer potential of isolated compounds.
Main Methods:
- Phytochemical investigation using molecular networking.
- Isolation and structure elucidation of compounds using spectroscopic data (NMR, ROESY).
- Cytotoxicity assays against human glioblastoma (U87) and lung (A549) cancer cell lines.
Main Results:
- Seven new prenylated stilbenes, schweinfurthins K-Q, were isolated and characterized.
- Known compounds vedelianin, schweinfurthins E-G, mappain, and methyl-mappain were also identified.
- The cytotoxic activities of all 13 isolated compounds were evaluated against U87 and A549 cell lines.
Conclusions:
- Macaranga tanarius yielded new prenylated stilbenes with potential cytotoxic properties.
- The study expands the known schweinfurthin series with novel chemical entities.
- Further investigation into the anticancer mechanisms of these compounds is warranted.
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