| Literature DB >> 24900565 |
Gaozhi Chen1, Zhiguo Liu1, Yali Zhang2, Xiaoou Shan3, Lili Jiang3, Yunjie Zhao1, Wenfei He1, Zhiguo Feng1, Shulin Yang2, Guang Liang1.
Abstract
Sepsis, an acute inflammatory disease, remains the most common cause of death in intensive care units. A series of benzimidazole and imidazopyridine derivatives were synthesized and screened for anti-inflammatory activities, and the imidazopyridine series showed excellent inhibition of the expression of inflammatory cytokines in LPS-stimulated macrophages. Compounds X10, X12, X13, X14, and X15 inhibited TNF-α and IL-6 release in a dose-dependent manner, and X12 showed no cytotoxicity in hepatic cells. Furthermore, X12 exhibited a significant protection against LPS-induced septic death in mouse models. Together, these data present a series of new imidazopyridines with potential therapeutic effects in acute inflammatory diseases.Entities:
Keywords: anti-inflammation; benzimidazoles; imidazopyridines; macrophages; sepsis
Year: 2012 PMID: 24900565 PMCID: PMC4027431 DOI: 10.1021/ml300282t
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345