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Synthesis, characterization and anticancer, antibacterial activities of pentacyclic triterpenoid glycoside derivatives.
Wang, Pan-Pan; Liu, Yan-Dan; Cui, Lan-Tian; Li, Gao; Zhao, Long-Xuan; Jin, Mei.
Afiliação
  • Wang PP; School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China.
  • Liu YD; School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China.
  • Cui LT; Key Laboratory of Natural Resources of Changbai Mountain and Functional Molecules, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, China.
  • Li G; Key Laboratory of Natural Resources of Changbai Mountain and Functional Molecules, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, China.
  • Zhao LX; School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China.
  • Jin M; Key Laboratory of Natural Resources of Changbai Mountain and Functional Molecules, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, China.
J Asian Nat Prod Res ; : 1-17, 2024 Sep 24.
Article em En | MEDLINE | ID: mdl-39317172
ABSTRACT
As a kind of glycoside, pentacyclic triterpenoid saponins have good biological activities, such as anticancer, antibacterial, antiviral and hypoglycemic effects [1]. In this paper, twenty-four pentacyclic triterpenoid derivatives, including twelve monosaccharide derivatives, were designed and synthesized. The anticancer effect and antibacterial activities of all compounds were evaluated. It is noteworthy that compound UA-2b has the strongest inhibitory effect on the growth of A549, Hela and HepG2 cancer cells (IC50 = 5.37 ± 0.22 µM, 5.82 ± 0.25 µM and 5.47 ± 0.06 µM, respectively). Compounds OA-2b, OA-6a, OA-6b, UA-2b and UA-6a have the best activity against Escherichia coli 1924 (MIC = 16 µg/ml).
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article