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Synthesis and biological evaluation of pentacyclic triterpenoid derivatives as potential novel antibacterial agents

2021; Elsevier BV; Volume: 109; Linguagem: Inglês

10.1016/j.bioorg.2021.104692

1090-2120

Panpan Wu, Borong Tu, Jinfeng Liang, Shengzhu Guo, Nana Cao, Silin Chen, Zhujun Luo, Jia-Hao Li, Wende Zheng, Xiaowen Tang, Dongli Li, Xue-Tao Xu, Wenfeng Liu, Xi Zheng, Zhaojun Sheng, Adam P. Roberts, Kun Zhang, W. David Hong,

Toxin Mechanisms and Immunotoxins

A series of ursolic acid (UA), oleanolic acid (OA) and 18β-glycyrrhetinic acid (GA) derivatives were synthesized by introducing a range of substituted aromatic side-chains at the C-2 position after the hydroxyl group at C-3 position was oxidized. Their antibacterial activities were evaluated in vitro against a panel of four Staphylococcus spp. The results revealed that the introduction of aromatic side-chains at the C-2 position of GA led to the discovery of potent triterpenoid derivatives for inhibition of both drug sensitive and resistant S. aureus, while the other two series derivatives of UA and OA showed no significant antibacterial activity even at high concentrations. In particular, GA derivative 33 showed good potency against all four Staphylococcus spp. (MIC = 1.25–5 μmol/L) with acceptable pharmacokinetics properties and low cytotoxicity in vitro. Molecular docking was also performed using S. aureus DNA gyrase to rationalize the observed antibacterial activity. This series of GA derivatives has strong potential for the development of a new type of triterpenoid antibacterial agent.