甘草查尔酮A的分布、生物合成、代谢和药理作用。

IF 1.8 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoxiao Wang, Jinrui Liu, Wei Li, Xingjie Tao, Chenxi Yu, Junbo Xie, Yanqing Zhang
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引用次数: 0

摘要

甘草查尔酮A (Licochalcone A, LCA)是甘草中重要的次生代谢物,因其独特的种特异性分布特征和多种药效学活性,特别是其抗炎和抗癌作用而受到广泛关注。LCA最初被认为是Glycyrrhiza inflata Batal独有的。然而,进一步的分析表明其分布在不同的甘草物种中,扩展了其在甘草物种中的已知分布,并表明其在次生代谢中起着更广泛的作用。然而,LCA的复杂化学合成在区域选择性控制方面提出了挑战。由于肠道首过效应,LCA的口服生物利用度有限,其代谢机制尚未完全阐明。这些问题限制了LCA在体内的治疗效果和实际应用。近年来,优化合成途径和开发新的给药系统的进展显著提高了LCA的疗效,同时在安全性方面也取得了显著突破。本文综述了LCA的分布规律、合成方法、体内代谢过程、药理作用及应用现状,并对今后的研究方向进行了展望。但其代谢机制及临床应用前景仍需进一步研究。多源数据库检索相关文献,以“Licochalcone A”为锚定词,协同物种分类学(Glycyrrhiza)、生物地理格局、植物化学动力学(生物合成/代谢)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive Insights into Licochalcone A: its Distribution, Biosynthesis, Metabolism, and Pharmacological Effects.

Licochalcone A (LCA) is an important secondary metabolite in licorice that has attracted extensive attention due to its unique species-specific distribution characteristics and various pharmacodynamic activities, particularly its anti-inflammatory and anti-cancer effects. LCA was originally considered exclusive to Glycyrrhiza inflata Batal. However, further analyses have shown its distribution in different licorice species, extending its known distribution among licorice species and suggesting a broader role in secondary metabolism. Nevertheless, the complex chemical synthesis of LCA presents challenges in regioselectivity control. The oral bioavailability of LCA is limited due to the intestinal first-pass effect, and its metabolic mechanism has not yet been fully elucidated. These issues restrict the therapeutic effects and practical applications of LCA in vivo. In recent years, advancements in optimizing synthetic pathways and developing new delivery systems have significantly improved the efficacy of LCA while also achieving notable breakthroughs in its safety. This review examines the distribution patterns, synthesis methods, in vivo metabolic processes, pharmacological activities, and current application status of LCA, while also exploring future research directions. However, its metabolic mechanisms and prospects for clinical application still require further investigation in the future. A multisource database search related literature employed "Licochalcone A"as the anchor term, synergized with species taxonomy (Glycyrrhiza), biogeographic patterns, and phytochemical dynamics (biosynthesis/metabolism).

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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