synthesis, molecular docking and biological evaluation of glycyrrhizin analogs as anticancer agents targeting egfr
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ID: 148121
2014
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Abstract
Glycyrrhizin (GA) analogs in the form of 3-glucuronides and 18-epimers were synthesized and their anticancer activities were evaluated. Alkaline isomerization of monoglucuronides is reported. In vitro and in vivo studies showed that glycyrrhetinic acid monoglucuronides (GAMGs) displayed higher anticancer activities than those of bisglucuronide GA analogs, while anticancer activity of the 18α-epimer was superior to that of the 18β-epimer. 18α-GAMG was firstly nicely bound to epidermal growth factor receptor (EGFR) via six hydrogen bonds and one charge interaction, and the docking calculation proved the correlation between anticancer activities and EGFR inhibitory activities. Highly active 18α-GAMG is thus of interest for the further studies as a potential anticancer agent.
| Reference Key |
yang2014moleculessynthesis,
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|---|---|
| Authors | ;Yong-An Yang;Wen-Jian Tang;Xin Zhang;Ji-Wen Yuan;Xin-Hua Liu;Hai-Liang Zhu |
| Journal | Journal of ethnopharmacology |
| Year | 2014 |
| DOI |
10.3390/molecules19056368
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