TXNIP公司
硫氧还蛋白相互作用蛋白
硫氧还蛋白
酚类
疾病
氧化应激
化学
生物化学
医学
内科学
作者
Meng Zhang,Guanhua Hu,Nan Shao,Yun-Peng Qin,Qian Chen,Yan Wang,Peng Zhou,Biao Cai
标识
DOI:10.1007/s10787-021-00861-4
摘要
Alzheimer's disease (AD) is a neurodegenerative disease characterized by amyloid plaques and tangles that have become the fifth leading cause of death worldwide. Previous studies have found that thioredoxin interacting protein (TXNIP) expression was increased during the development of AD neurons. TXNIP separates from the TXNIP-thioredoxin complex, and the TXNIP-NLRP3 complex assembles ASC and pro-caspase-1 to form the NLRP3 inflammasome, which triggers AD inflammation and apoptosis. CB-dock was used to explore whether 21 natural flavonoids and phenols target TXNIP based on references. Docking results showed that rutin, puerarin, baicalin, luteolin and quercetin are the most potent TXNIP inhibitors, and among them, rutin as the most effective flavonoid. And rosmarinic acid is the most potent TXNIP inhibitor of phenols. These phytochemicals could be helpful to find the lead compounds in designing and developing novel agents for Alzheimer's disease.
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