Design and Synthesis of Novel 3β-O-Succinyl-lupeol and 3β-O-Maleicyl-lupeol Derivatives as Potential Antitumor Agents

Lupeol is a natural pentacyclic triterpenoid with a wide range of biological activities. To enhance the antitumor efficacy of lupeol, eight lupeol-3-succinate derivatives and seven lupeol-3-maleate derivatives were designed and synthesized. The new compounds were evaluated for their cytotoxic activities against human lung cancer A549 cell line, human liver cancer HepG2 cell line, and human breast cancer MCF-7 cell line. All compounds were found to show better cytotoxic activity in vitro than lupeol. Among them, lup-20(29)-en-3β-yl 4-oxo-4-(pyrrolidin-1-yl)butanoate displayed remarkable cytotoxic activity against lung cancer A549 cells, with an IC50 of 2.33 μM, and potently induced apoptosis in lung cancer A549 cells. The mechanism of action of lup-20(29)-en-3β-yl 4-oxo-4-(pyrrolidin-1-yl)butanoate can be subjected to further evaluation. It has potential to become a novel anti-tumor agent through further structural modification.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2024-11-01
DOI
https://doi.org/10.1134/s1070363224110203
Citations
2
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.47
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article

Design and Synthesis of Novel 3β-O-Succinyl-lupeol and 3β-O-Maleicyl-lupeol Derivatives as Potential Antitumor Agents

Ran Luo, Xin Hong, Yu Han, Juanjuan Song et al.
2 citations
Russian Journal of General Chemistry
Natural product bioactivities and synthesis
0.47
article

Design and Synthesis of Novel 3β-O-Succinyl-lupeol and 3β-O-Maleicyl-lupeol Derivatives as Potential Antitumor Agents

Ran Luo, Xin Hong, Yu Han, Juanjuan Song, Haining Cui, Ming Bu, Zhixin Chen, Michael L. Wang, Tianhong Xu
article en
2 citations

Abstract

Lupeol is a natural pentacyclic triterpenoid with a wide range of biological activities. To enhance the antitumor efficacy of lupeol, eight lupeol-3-succinate derivatives and seven lupeol-3-maleate derivatives were designed and synthesized. The new compounds were evaluated for their cytotoxic activities against human lung cancer A549 cell line, human liver cancer HepG2 cell line, and human breast cancer MCF-7 cell line. All compounds were found to show better cytotoxic activity in vitro than lupeol. Among them, lup-20(29)-en-3β-yl 4-oxo-4-(pyrrolidin-1-yl)butanoate displayed remarkable cytotoxic activity against lung cancer A549 cells, with an IC50 of 2.33 μM, and potently induced apoptosis in lung cancer A549 cells. The mechanism of action of lup-20(29)-en-3β-yl 4-oxo-4-(pyrrolidin-1-yl)butanoate can be subjected to further evaluation. It has potential to become a novel anti-tumor agent through further structural modification.

Russian Journal of General ChemistryVol. 94(11)
Qiqihar Medical University (CN)
Zero hunger
Openalex Percentile: Top 33%
Natural product bioactivities and synthesis
0.47
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