高尿酸血症
痛风
化学
非布索坦
黄嘌呤氧化酶
尿酸
药理学
毒性
生物化学
医学
有机化学
酶
作者
Xiaoyi Zeng,Yajing Liu,Yuxin Fan,Di Wu,Yangyang Meng,Mingze Qin
标识
DOI:10.1021/acs.jmedchem.3c01710
摘要
Gout is characterized by hyperuricemia and the deposition of monosodium urate (MSU) crystals around joints. Despite the availability of several drugs on the market, its treatment remains challenging owing to the notable side effects, such as hepatorenal toxicity and cardiovascular complications, that are associated with most existing agents. This perspective aims to summarize the current research progress in the development of antigout agents, particularly focusing on xanthine oxidase (XO) and urate anion transporter 1 (URAT1) inhibitors from a medicinal chemistry viewpoint and their preliminary structure–activity relationships (SARs). This perspective provides valuable insights and theoretical guidance to medicinal chemists for the discovery of antigout agents with novel chemical structures, better efficiency, and lower toxicity.
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