Glycoalkaloids: Structural diversity and pharmacological activities

Author:

Jia Yuelin12,Xia Guiyang134,Wang Lingyan1,Xia Huan1,Wei Xiaohong1,Lin Sheng13

Affiliation:

1. Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China

2. Wuya Innovation College, Shenyang Pharmaceutical University, Shenyang, China

3. College of Pharmaceutical Sciences, Qinghai University for Nationalities, Xining, China

4. College of Eco-Environmental Engineering, Qinghai University, Xining, China

Abstract

Glycoalkaloids (GAs) are a class of special secondary metabolites found in plants. Studies have found that they have a wide range of pharmacological activities, such as antiviral, antifungal, and anticancer properties, with significant potential for development and utilization value. At present, alkaloid glucosides mainly fall into 2 categories: indole alkaloid glucosides and steroid alkaloid glucosides. In addition, there are small amounts of quinolines, isoquinolines, isoguanines, and other alkaloids. At present, only a few of the GAs have been found, which is inconsistent with the diversity of alkaloids. In addition, only a few GAs have been isolated and identified. This paper reviews the natural alkaloid glycosides from the perspectives of structural classification and pharmacological activity. It analyzes the reasons for the limited number of isolated components and proposes a rational separation method based on the literature. To provide references for the separation, identification, and bioactivity of glycoalkaloids.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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