体内
炎症
TLR4型
MAPK/ERK通路
化学
下调和上调
药理学
体外
类黄酮
结构-活动关系
肿瘤坏死因子α
信号转导
生物化学
医学
生物
免疫学
基因
生物技术
抗氧化剂
作者
Yun Xiao,Yaoyao Yan,Juncheng Du,Xiaoxiao Feng,Famin Zhang,Xu Han,Yong Hu,Xinhua Liu
标识
DOI:10.1080/14756366.2022.2124983
摘要
It is significant to design, synthesise and optimise flavonoid derivatives with better anti-inflammatory activity. This study aims to design and synthesise a series of novel 2-phenyl-4H-chromen-4-one compounds with anti-inflammatory; among them, compound 8 was discovered as the best one. And then, the effects of compound 8 on the TLR4/MAPK signalling pathway was carried out in vivo, the results indicated that compound 8 could downregulate NO, IL-6, and TNF-α expression, and suppress LPS-induced inflammation by inhibiting the TLR4/MAPK pathways. Furthermore, compound 8 reduced inflammation by a mouse model of LPS-induced inflammatory disease in vivo. The results suggest that compound 8 has the potential against inflammation through regulating TLR4/MAPK pathway and can be assessed further for drug development.
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