Nimbus Therapeutics, 22 Boston Wharf Road, Floor 9, Boston, Massachusetts 02210, United States.
J Med Chem. 2024 Oct 24;67(20):18017-18021. doi: 10.1021/acs.jmedchem.4c02264. Epub 2024 Oct 7.
IRAK4 inhibitors have been sought for the treatment of a host of diseases, however, recent evidence suggests a protein degradation approach might have advantages over an inhibitor. This viewpoint summarizes the discovery of KT-474─a selective and orally bioavailable interleuken receptor-associated kinase 4 proteolysis-targeting chimera in Phase 2 clinical trials for autoimmune indications.
IRAK4 抑制剂已被广泛用于治疗多种疾病,但最近的证据表明,蛋白降解方法可能优于抑制剂。本文观点总结了 KT-474 的发现,这是一种选择性、口服生物可利用的白细胞介素受体相关激酶 4 蛋白水解靶向嵌合体,目前正在进行自身免疫适应症的 2 期临床试验。