黄嘌呤氧化酶抑制剂的过去、现在和未来:设计策略、结构和药理学见解、专利和临床试验

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
MedChemComm Pub Date : 2023-08-07 DOI:10.1039/D3MD00316G
Atamjit Singh, Karanvir Singh, Aman Sharma, Kirandeep Kaur, Renu Chadha and Preet Mohinder Singh Bedi
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引用次数: 0

摘要

黄嘌呤氧化酶,钼黄酶和黄嘌呤脱氢酶的异构体都作为黄嘌呤氧化还原酶存在,并负责嘌呤的分解代谢。黄嘌呤氧化酶在广泛调节时更多地参与病理条件。黄嘌呤氧化酶的升高不仅是痛风的主要原因,而且还负责各种高尿酸血症相关的病理状况,如糖尿病,慢性伤口,心血管疾病,阿尔茨海默病等。目前临床使用的黄嘌呤氧化酶抑制剂(别嘌呤醇、非布司他和托吡司他)存在致命的副作用,给医疗保健系统带来了严重的问题,促使全球迫切需要开发新型、有效和更安全的黄嘌呤氧化酶抑制剂。本综述将提供关键和系统的信息:a.设计策略(灵感来自临床实践中的上市药物和天然产品),结构见解和药理学输出(黄嘌呤氧化酶抑制和相关活性)在过去二十年中由全球各个研究小组报告的各种临床前候选药物;B.在过去三十年中发表的专利黄嘌呤氧化酶抑制剂和c.临床试验及其批准的候选药物的结果。这篇综述中产生的信息表明,基于片段的药物设计(FBDD)和分子杂交技术最适合开发所需的黄嘌呤氧化酶抑制剂,因为它们一方面对酶具有高选择性,另一方面赋予结构多功能特性,并且两者都可能具有超越现有临床药物限制的能力。所有这些结合将专门更新黄嘌呤氧化酶抑制剂和相关领域的研究人员,并可能有助于设计合理、新颖、有效和更安全的黄嘌呤氧化酶抑制剂,有效地解决黄嘌呤氧化酶相关疾病和障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Past, present and future of xanthine oxidase inhibitors: design strategies, structural and pharmacological insights, patents and clinical trials

Past, present and future of xanthine oxidase inhibitors: design strategies, structural and pharmacological insights, patents and clinical trials

Xanthine oxidase, a molybdo-flavoenzyme, and an isoform of xanthine dehydrogenase both exist as xanthine oxidoreductase and are responsible for purine catabolism. Xanthine oxidase is more involved in pathological conditions when extensively modulated. Elevation of xanthine oxidase is not only the prime cause of gout but is also responsible for various hyperuricemia associated pathological conditions like diabetes, chronic wounds, cardiovascular disorders, Alzheimer's disease, etc. Currently available xanthine oxidase inhibitors in clinical practice (allopurinol, febuxostat and topiroxostat) suffer from fatal side effects that pose a serious problem to the healthcare system, raising global emergency to develop novel, potent and safer xanthine oxidase inhibitors. This review will provide key and systematic information about: a. design strategies (inspired from both marketed drugs in clinical practice and natural products), structural insights and pharmacological output (xanthine oxidase inhibition and associated activities) of various pre-clinical candidates reported by various research groups across the globe in the past two decades; b. patented xanthine oxidase inhibitors published in the last three decades and c. clinical trials and their outcomes on approved drug candidates. Information generated in this review has suggested fragment-based drug design (FBDD) and molecular hybridization techniques to be most suitable for development of desired xanthine oxidase inhibitors as one provides high selectivity toward the enzyme and the other imparts multifunctional properties to the structure and both may possess capabilities to surpass the limitations of currently available clinical drugs. All in combination will exclusively update researchers working on xanthine oxidase inhibitors and allied areas and potentially help in designing rational, novel, potent and safer xanthine oxidase inhibitors that can effectively tackle xanthine oxidase related disease conditions and disorders.

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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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