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甘草次酸的治疗潜力:专利研究综述(2010-2017)。

Therapeutic potential of glycyrrhetinic acids: a patent review (2010-2017).

机构信息

a Department of Bioorganic Chemistry , Leibniz Institute of Plant Biochemistry , Halle (Saale) , Germany.

b UoN Chair of Oman's Medicinal Plants and Marine Natural Products , University of Nizwa , Nizwa , Sultanate of Oman.

出版信息

Expert Opin Ther Pat. 2018 May;28(5):383-398. doi: 10.1080/13543776.2018.1455828. Epub 2018 Mar 26.

Abstract

INTRODUCTION

Glycyrrhetinic acids (GAs) viz., 18β-glycyrrhetinic acid and 18α-glycyrrhetinic acid, are oleanane-type triterpenes having a carboxylic acid group at C-30, and are extracted from the Chines herbal medicine licorice (Glycyrrhiza uralensis). Although the pharmacological properties of GAs have long been known, attention to them has greatly increased in recent times due to their cytotoxic activity.

AREAS COVERED

This review represents the patents granted about natural and synthetic glycyrrhetinic acid analogs from January 2010 to December 2017, the advances made by research groups in conjunction with pharmaceutical companies in the discovery of new natural or synthetic glycyrrhetinic acid analogs.

EXPERT OPINION

GAs demonstrate excellent cytotoxic, antimicrobial, enzyme inhibitory, antiinflammatory, antioxidant, analgesic, and antiviral effects. It is interesting to note that the C-(OH) and CCOH functional groups make GAs very attractive lead structures for medicinal scientists since these functionalities allow the generation of further chemical diversity for improved pharmacological effects. Moreover, various GA analogues have been prepared via modification of the CCOH. It is noteworthy that the C-30 amide of GA demonstrated better cytotoxic effects compared to the parent compounds. In addition, GAs have the capability to conjugate with other anticancer drugs or be converted into their halo or amino analogs which is expected to stimulate medicinal chemist to synthesize new lead compounds in cancer drug discovery.

摘要

简介

甘草次酸(GA),即 18β-甘草次酸和 18α-甘草次酸,是一种具有 C-30 羧酸基团的齐墩果烷型三萜,从中药甘草(甘草)中提取。尽管 GA 的药理性质早已为人所知,但由于其细胞毒性活性,近年来人们对它们的关注大大增加。

涵盖领域

本综述代表了 2010 年 1 月至 2017 年 12 月期间授予的天然和合成甘草次酸类似物专利,以及研究小组与制药公司在发现新的天然或合成甘草次酸类似物方面取得的进展。

专家意见

GA 表现出优异的细胞毒性、抗菌、酶抑制、抗炎、抗氧化、镇痛和抗病毒作用。有趣的是,C-(OH)和 CCOH 官能团使 GA 成为药物科学家非常有吸引力的先导结构,因为这些官能团允许产生更多的化学多样性,以提高药理作用。此外,已经通过修饰 CCOH 制备了各种 GA 类似物。值得注意的是,与母体化合物相比,GA 的 C-30 酰胺表现出更好的细胞毒性作用。此外,GA 能够与其他抗癌药物结合,或转化为其卤代或氨基类似物,预计这将激发药物化学家在癌症药物发现中合成新的先导化合物。

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