Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Science, Nanjing Normal University, Nanjing, China.
Basic Clin Pharmacol Toxicol. 2009 Nov;105(5):350-6. doi: 10.1111/j.1742-7843.2009.00463.x. Epub 2009 Sep 8.
2-(4-Aminophenyl)-3-(3,5-dihydroxylphenyl) propenoic acid (CSN-07001) is a new compound based on the combination of resveratrol and propenoic acid derivatives. In vitro cyclooxygenase (COX)/5-lipoxygenase (5-LOX) inhibition assays showed that the test compound exhibited a dual inhibitory activity against the COX (COX-1 IC(50) = 2.20 microM, COX-2 IC(50) = 1.76 microM) and 5-LOX (IC(50) = 0.28 microM) enzymes. Further, the enhanced COX-1/COX-2/5-LOX expression in lipopolysaccaride-induced lung inflammation in mice was also suppressed by CSN-07001 in a concentration-dependent manner. In vivo studies showed that CSN-07001 exhibited potent anti-inflammatory and antinociceptive effects in different experimental models. We further examined the risk of gastric damage induced by CSN-07001. The test compound was gastric-sparing in that it elicited markedly fewer stomach lesions than indomethacin in rats. Taken together, our data indicate that CSN-07001 exhibits a novel class of dual inhibitors of COX and 5-LOX having therapeutic potential as non-steroidal anti-inflammatory agents with an enhanced gastric safety profile.
2-(4-氨基苯基)-3-(3,5-二羟基苯基)丙烯酸(CSN-07001)是一种基于白藜芦醇和丙烯酸衍生物结合的新型化合物。体外环氧化酶(COX)/5-脂氧合酶(5-LOX)抑制试验表明,该测试化合物对 COX(COX-1 IC(50)= 2.20 μM,COX-2 IC(50)= 1.76 μM)和 5-LOX(IC(50)= 0.28 μM)具有双重抑制活性。此外,CSN-07001 还可浓度依赖性地抑制脂多糖诱导的小鼠肺部炎症中 COX-1/COX-2/5-LOX 的表达增强。体内研究表明,CSN-07001 在不同的实验模型中表现出强大的抗炎和镇痛作用。我们进一步检查了 CSN-07001 引起的胃损伤风险。与吲哚美辛相比,该测试化合物具有胃保护作用,可明显减少大鼠的胃损伤。总之,我们的数据表明 CSN-07001 具有新型的 COX 和 5-LOX 双重抑制剂作用,作为非甾体抗炎药具有治疗潜力,同时具有增强的胃安全性。