HDAC6型
化学
组蛋白脱乙酰基酶
炎症性肠病
炎症体
结肠炎
组蛋白
炎症
药理学
生物化学
癌症研究
乙酰化
HDAC1型
细胞生物学
药代动力学
合理设计
组蛋白脱乙酰基酶2
对接(动物)
HDAC4型
信号转导
小分子
结构-活动关系
作者
Simin Sun,Kairui Yue,Enqiang Liu,Danmei Sheng,Yuxin Chen,Tianqi Li,Aijun Shen,Geng Jia,Yuqi Jiang,Xiaoyang Li
标识
DOI:10.1021/acs.jmedchem.5c02554
摘要
Histone deacetylase 6 (HDAC6) modulates inflammatory signaling through both its catalytic domain and its zinc-finger ubiquitin-binding domain, which makes inhibiting HDAC6 a promising anti-inflammatory therapeutic strategy. Previously, we developed a series of hydrazide-based HDAC6-selective inhibitors with favorable pharmacokinetic properties. Based on this, we herein report the rational design and synthesis of first-in-class hydrazide-based HDAC6 degraders that eliminate both the catalytic and zinc-finger ubiquitin-binding domain. Among them, compound 22f (DC50 = 13.4 nM) potently and selectively degraded HDAC6 via the ubiquitin-proteasome pathway without impacting other HDAC subtypes and CRBN neosubstrates. 22f inhibits NLRP3 inflammasome assembly and activation, as well as blocks NF-κB signaling, thereby reducing the transcription and release of key inflammatory factors. In a DSS-induced mouse colitis model, 22f significantly mitigated disease symptoms and histopathological damage. Overall, this study validated the potential of hydrazide-based HDAC6 PROTAC molecules for the treatment of inflammatory bowel disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI