首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and biological evaluation of novel dimethyl(1,1'-biphenyl)-2,2'-dicarboxylate derivatives containing thiazolidine-2,4-dione for the treatment of concanavalin A-induced acute liver injury of BALB/c mice.
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Synthesis and biological evaluation of novel dimethyl(1,1'-biphenyl)-2,2'-dicarboxylate derivatives containing thiazolidine-2,4-dione for the treatment of concanavalin A-induced acute liver injury of BALB/c mice.

机译:含有噻唑烷-2,4-二酮的新型二甲基(1,1'-联苯)-2,2'-二羧酸二甲酯衍生物的合成和生物学评价,用于治疗伴刀豆球蛋白A引起的BALB / c小鼠急性肝损伤。

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In this paper, we reported the synthesis of bifendate derivatives and evaluation of anti-inflammatory activity by detecting the production of the Nitric Oxide (NO) in the lipopolysaccharide(LPS)-stimulated RAW 264.7 cell lines. Among the newly derivatives, compound 7k was the most potent one and two other compounds (7e and 7f) also exhibited greater anti-inflammatory activity than bifendate. Further in vivo studies confirmed that 7k significantly and dose-dependently inhibited carrageenan-induced paw edema and decreased the serum levels of alanine aminotransaminase, and aspartate aminotransaminase in concanavalin A-induced hepatitis model. Histopathological evaluation demonstrated that 7k has better hepatoprotective effect on acute liver injury induced by concanavalin A than bifendate, suggesting that 7k is a potential drug candidate for the treatment of hepatic injuries.
机译:在本文中,我们通过检测脂多糖(LPS)刺激的RAW 264.7细胞系中一氧化氮(NO)的产生,报告了联苯二酸酯衍生物的合成和抗炎活性的评估。在新衍生物中,化合物7k是最有效的一种,另外两种化合物(7e和7f)也显示出比联苯菊酯更大的抗炎活性。进一步的体内研究证实,在伴刀豆球蛋白A诱发的肝炎模型中,7k显着且剂量依赖性地抑制角叉菜胶诱导的爪水肿并降低血清丙氨酸氨基转氨酶和天冬氨酸氨基转氨酶的水平。组织病理学评估表明,7k对伴刀豆球蛋白A引起的急性肝损伤的保护作用优于联苯双酯,这表明7k是治疗肝损伤的潜在候选药物。

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