苯并咪唑
消炎药
化学
炎症
药理学
天然产物
NF-κB
地塞米松
生物化学
生物
医学
免疫学
有机化学
信号转导
内科学
作者
Qiongyu Zhang,Jun-Xiao Hu,Xu Kui,Chao Liu,Hui Zhou,Xiaoxin Jiang,Leping Zeng
出处
期刊:PubMed
[National Institutes of Health]
日期:2017-01-01
卷期号:16 (4): 1405-1414
被引量:12
摘要
Transcription factor NF-κB and relevant cytokines IL-6 and IL-8 play a pivotal role in the pathogenesis of inflammation. Sinapic acid is a natural product and was demonstrated to possess anti-inflammatory activity. In this paper, we synthesized a series of sinapic acid derivatives and evaluated their anti-inflammatory effects. The result suggested that all of the targets compounds 7a-j inhibit NF-κB activation and decrease IL-6 and IL-8 expression in BEAS-2B cells. By our biological assays, we found that all of the prepared compounds displayed stronger anti-inflammatory activities than their precursor sinapic acid. Especially, compounds 7g and 7i, with electron-drawing groups (nitro and fluoro moieties) in the benzimidazole ring, exhibited remarkable anti-inflammation activity, which was even stronger than the reference drug dexamethasone.
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