Binding uric acid: a pure chemical solution for the treatment of hyperuricemia.
Yun-Yun LiJing LiYan LiHong-Ping LongWei LinYi-Kun WangRong TangXue-Wu LiuDejian JiangShao LiuDong-Sheng CaoGui-Shan TanKang-Ping XuWen-Xuan WangPublished in: RSC advances (2024)
Hyperuricemia, characterized by elevated uric acid levels and subsequent crystal deposition, contributing to conditions such as gout, cardiovascular events, and kidney injury, poses a significant health threat, particularly in developed countries. Current drug options for treatment are limited, with safety concerns, leading to suboptimal therapeutic outcomes in symptomatic hyperuricemia patients and a lack of pharmaceutical interventions for asymptomatic cases. Distinguishing from the previous drug design strategies, we directly target uric acid, the pathological molecule of hyperuricemia, resulting in a pyrimidine derivative capable of increasing the solubility and excretion of uric acid by forming a complex with it. Its prodrug showed an anti-hyperuricemia activity comparable to benzbromarone and a favorable safety profile in vivo . Our finding provides a strategy purely based on organic chemistry to address the largely unmet therapeutic needs on novel anti-hyperuricemia drugs.
Keyphrases
- uric acid
- metabolic syndrome
- cardiovascular events
- end stage renal disease
- public health
- healthcare
- chronic kidney disease
- cardiovascular disease
- newly diagnosed
- physical activity
- ejection fraction
- mental health
- emergency department
- peritoneal dialysis
- drug induced
- type diabetes
- health information
- risk assessment
- adverse drug
- binding protein
- patient reported
- human health