转化式学习
重要事件
计算生物学
生物信息学
化学
疾病
药物开发
透视图(图形)
药物发现
医学
生长激素
激素
神经科学
药理学
癌症研究
作者
Jingwei Li,Ruixian Chen,Jinhang Zhang,Jinhan He,Yuxi Wang,Yanping Li
标识
DOI:10.1021/acs.jmedchem.5c03114
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as a critical global public health challenge, with limited therapeutic options underscoring the necessity for innovative therapies. Thyroid hormone receptor-β (THR-β), the predominant THR isoforms in the liver, plays a pivotal role in regulating lipid homeostasis, inflammation, and hepatic fibrosis, positioning it as a compelling therapeutic target. Although early THR-β agonists have demonstrated potential, their clinical application was restricted by systemic side effects and poor THR-β selectivity. Advances in medical chemistry have now developed highly selective THR-β with improved potency. The recent FDA approval of Resmetirom (MGL-3196), a liver-targeted THR-β agonist, represents a transformative milestone in MASLD pharmacotherapy. This perspective examines MASLD pathogenesis and current therapeutic landscape, elucidates the biological functions and structural features of THR-β, and critically evaluates existing and emerging THR-β agonists. Additionally, we highlight breakthroughs in selective THR-β agonists development and discuss future directions for optimizing THR-β-targeted therapies.
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