化学
黄嘌呤氧化酶
效力
部分
立体化学
体内
对接(动物)
体外
蒽醌
生物化学
药理学
组合化学
酶
有机化学
医学
生物
护理部
生物技术
作者
Shuai Guo,Qi Sun,Xu Zhang,Songye Li,H. Liu,Gong-hui Ge,Jing Wang,Xing‐yang Liu,Ben Xu,Tingting Li,Xianfeng Zhou,Yanping Wang,Fan‐hao Meng,Ting‐jian Zhang
标识
DOI:10.1002/ardp.202400137
摘要
In our previous study, we reported a series of N-(9,10-anthraquinone-2-carbonyl) amino acid derivatives as novel inhibitors of xanthine oxidase (XO). Recognizing the suboptimal drug-like properties associated with the anthraquinone moiety, we embarked on a nonanthraquinone medicinal chemistry exploration in the current investigation. Through systematic structure-activity relationship (SAR) studies, we identified a series of 4-(isopentyloxy)-3-nitrobenzamide derivatives exhibiting excellent in vitro potency against XO. The optimized compound, 4-isopentyloxy-N-(1H-pyrazol-3-yl)-3-nitrobenzamide (6k), demonstrated exceptional in vitro potency with an IC
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