喹啉
伤亡人数
药物发现
Toll样受体
药理学
计算机科学
数据科学
医学
计算生物学
受体
化学
生物信息学
生物
免疫学
内科学
先天免疫系统
有机化学
作者
Xue Song,Chen‐Guo Feng,Chen Wang,Jie‐Fei Cheng,Guo‐Qiang Lin
标识
DOI:10.1021/acsmedchemlett.5c00248
摘要
The Toll-like receptor (TLR) family are critical components of the innate immune system, acting as pattern recognition receptors that detect microbial components and initiate immune responses. In humans, 10 TLRs have been identified, each recognizing distinct pathogen-associated molecular patterns. Among these, TLR9 is unique in its ability to sense CpG motifs, playing a crucial role in the detection of bacterial and viral DNA. Despite its significance, targeting TLR9 for therapeutics has proven to be challenging. Herein we describe the discovery of a series of potent and selective TLR9 antagonists, represented by 5-(hexahydropyrrolo-[3,4-b]-pyrrol-1-(2H)-yl)-quinoline (38), with an IC50 value of 0.1 nM against hTLR9 and >10,000-fold selectivity over hTLR2/4/5/7/8. Compound 38 demonstrated good pharmacokinetic and excellent pharmacodynamic features, indicating its potential utility as a pharmacological tool and a therapeutic candidate for TLR9 related disorders.
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