王雪凝, 孔建强. 生物催化介导的葛根素衍生化研究进展J. 药学学报, 2020,55(7): 1590-1603. doi: 10.16438/j.0513-4870.2020-0308
引用本文: 王雪凝, 孔建强. 生物催化介导的葛根素衍生化研究进展J. 药学学报, 2020,55(7): 1590-1603. doi: 10.16438/j.0513-4870.2020-0308
WANG Xue-ning, KONG Jian-qiang. Research progress on the puerarin derivatization through biocatalysisJ. Acta Pharmaceutica Sinica, 2020,55(7): 1590-1603. doi: 10.16438/j.0513-4870.2020-0308
Citation: WANG Xue-ning, KONG Jian-qiang. Research progress on the puerarin derivatization through biocatalysisJ. Acta Pharmaceutica Sinica, 2020,55(7): 1590-1603. doi: 10.16438/j.0513-4870.2020-0308

生物催化介导的葛根素衍生化研究进展

Research progress on the puerarin derivatization through biocatalysis

  • 摘要: 葛根素药理活性多样,临床上常用于心脑血管疾病的治疗,但也存在水溶解性差、生物利用度低等问题。结构修饰是改善药物性质的一种重要方法,基于酶法合成的生物催化因其高选择性而成为葛根素结构修饰的主要途径之一。迄今为止,生物催化可以实现葛根素的酰化、糖基化和羟基化等修饰,已开发出多种水溶解性和生物利用度得到改善的活性葛根素衍生物。本文以修饰基团为导向,综述了将全细胞和工具酶作为生物催化剂获得葛根素衍生物的研究进展,以期为葛根素类药物的进一步合成、开发提供新思路。

     

    Abstract: Puerarin, also known as daidzein 8-C-glucoside, is a major isoflavone glycoside from Pueraria lobata. Puerarin has been shown to possess a variety of pharmacological activities. It has been widely used for the treatment of cardiovascular and cerebrovascular diseases. However, the further applications are limited due to its low water solubility and poor bioavailability. Structural modification is thus regarded as an efficient approach to improve the solubility and bioavailability of puerarin. Unlike chemical modifications, enzyme-assisted modifications, namely biocatalysis, is a promising alternative for the regioselective synthesis of puerarin derivatives due to its high selectivity. Up to date, acylation, glycosylation and hydroxylation of puerarin had been achieved through enzyme-based biocatalysis. Diverse active puerarin derivatives with improved solubility and bioavailability have been thus developed. Based on modification groups, this paper focused on the progress in the preparation of puerarin derivatives by biocatalysis, in which the whole-cells or pure enzymes were used as the biocatalysts. This article was expected to provide new ideas for the synthesis and development of puerarin drugs.

     

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