Lv Junwei, Sharma Alok, Zhang Ting, Wu Yuchen, Ding Xianting
1 School of Biomedical Engineering, Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, China.
SLAS Technol. 2018 Apr;23(2):111-127. doi: 10.1177/2472630317751840. Epub 2018 Jan 23.
Natural triterpenes represent a group of pharmacologically active and structurally diverse organic compounds. The focus on these phytochemicals has been enormous in the past few years, worldwide. Asiatic acid (AA), a naturally occurring pentacyclic triterpenoid, is found mainly in the traditional medicinal herb Centella asiatica. Triterpenoid saponins, which are the primary constituents of C. asiatica, are commonly believed to be responsible for their extensive therapeutic actions. Published research work has described the molecular mechanisms underlying the various biological activities of AA and its derivatives, which vary for each chronic disease. However, a compilation of the various pharmacological properties of AA has not yet been done. Herein, we describe in detail the pharmacological properties of AA and its derivatives that inhibit multiple pathways of intracellular signaling molecules and transcription factors that are involved in the various stages of chronic diseases. Furthermore, the pharmacological activities of AA were compared with two natural compounds: curcumin and resveratrol. This review summarizes the research on AA and its derivatives and helps to provide future directions in the area of drug development.
天然三萜类化合物是一类具有药理活性且结构多样的有机化合物。在过去几年里,全球范围内对这些植物化学物质的关注极大。积雪草苷(AA)是一种天然存在的五环三萜类化合物,主要存在于传统草药积雪草中。三萜皂苷是积雪草的主要成分,通常认为它们具有广泛的治疗作用。已发表的研究工作描述了AA及其衍生物各种生物活性的分子机制,这些机制因每种慢性病而异。然而,尚未对AA的各种药理特性进行汇编。在此,我们详细描述了AA及其衍生物的药理特性,它们可抑制参与慢性病各个阶段的细胞内信号分子和转录因子的多种途径。此外,还将AA的药理活性与两种天然化合物姜黄素和白藜芦醇进行了比较。本综述总结了对AA及其衍生物的研究,并有助于为药物开发领域提供未来方向。