Synthesis and cytotoxicity of the conjugates of diterpenoid isosteviol and -acetyl-D-glucosamine.

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ID: 81116
2019
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Abstract
A series of conjugates of diterpenoid isosteviol (16-oxo--beyeran-19-oic acid) and -acetyl-D-glucosamine was synthesised and their cytotoxicity against several human cancer cell lines (M-Hela, MCF-7, Hep G2, Panc-1, PC-3), as well as normal human cell lines (WI-38, Chang liver) was assayed. Most of the conjugates were found to be cytotoxic against the mentioned cancer cell lines in the range of IC values 13-89 µM. Two lead compounds and showed selective cytotoxicity against M-Hela (IC 13 and 14 µM) that was two times as high as the cytotoxicity of the anti-cancer drug Tamoxifen in control (IC 28 µM). It was found that cytotoxic activity of the lead compounds against M-Hela cells is due to induction of apoptosis.
Reference Key
garifullin2019synthesisnatural Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Garifullin, Bulat F;Strobykina, Irina Yu;Khabibulina, Leysan R;Sapunova, Anastasiya S;Voloshina, Aleksandra D;Sharipova, Radmila R;Khairutdinov, Bulat I;Zuev, Yuriy F;Kataev, Vladimir E;
Journal Natural product research
Year 2019
DOI
10.1080/14786419.2019.1650355
URL
Keywords
Cytotoxicity diterpenoids conjugates isosteviol n-acetyl-d-glucosamine

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