Identification and bioactivity evaluation of twelve previously undescribed depsidone derivatives from Garcinia oligantha.

Phytochemistry

Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, 110016, China. Electronic address:

Published: November 2024

AI Article Synopsis

  • Research on Garcinia oligantha Merr. revealed twelve new depsidone derivatives, named oliganthdepsidones A-L, identified through various spectroscopic techniques.
  • Oliganthdepsidone F demonstrated significant cytotoxic effects against multiple human cancer cell lines, with the strongest effects noted in HepG2 and A375 cells, showing IC values as low as 10.92 μM.
  • The compound was found to induce apoptosis, inhibit cell proliferation, and reduce migration and invasion in cancer cells, indicating potential as a therapeutic agent against certain cancers.

Article Abstract

Phytochemical studies on the leaves and twigs of Garcinia oligantha Merr. led to the isolation of twelve previously undescribed depsidone derivatives (oliganthdepsidones A-L, 1-12). Their structures were elucidated by extensive spectroscopic analysis including H and C NMR, HSQC, HMBC and NOESY along with HRESIMS. The structures of oliganthdepsidones G and J were finally determined using DFT-NMR chemical shift calculations and DP4+ methods. Cytotoxicity test in four human cancer cell lines indicated that oliganthdepsidone F had relatively strong cytotoxic effect against A375 (melanoma), A549 (lung cancer), HepG2 (liver cancer), and MCF-7 (breast cancer) cell lines with IC of 18.71, 15.44, 10.92, and 15.90 μM, respectively. The dose- and time-dependent antiproliferative effects of oliganthdepsidone F on these cell lines were also observed by CCK-8 test. As determined by fluorescent microscopy and flow cytometry in these cell lines, oliganthdepsidone F could promote cell apoptosis, leading to the inhibition of cell proliferation. The results of wound healing assay and transwell assay showed that oliganthdepsidone F could inhibit the migration and invasion of A549 and MCF-7 cell lines in a concentration-dependent manner.

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http://dx.doi.org/10.1016/j.phytochem.2024.114227DOI Listing

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