化学
可药性
调节器
硫氧还蛋白
药物发现
生物化学
共价键
计算生物学
酶
药理学
生物
基因
有机化学
作者
Matteo Ardini,Samuel Yaw Aboagye,Valentina Petukhova,Irida Kastrati,Rodolfo Ippoliti,Gregory R. J. Thatcher,Pavel A. Petukhov,David L. Williams,Francesco Angelucci
标识
DOI:10.1021/acs.jmedchem.4c00669
摘要
Pyridine nucleotide-disulfide oxidoreductases are underexplored as drug targets, and thioredoxin reductases (TrxRs) stand out as compelling pharmacological targets. Selective TrxR inhibition is challenging primarily due to the reliance on covalent inhibition strategies. Recent studies identified a regulatory and druggable pocket in
科研通智能强力驱动
Strongly Powered by AbleSci AI