Shrestha Suja, Bhattarai Bharat Raj, Lee Keun-Hyeung, Cho Hyeongjin
Department of Chemistry and Institute of Molecular Cell Biology, College of Natural Sciences, Inha University, Incheon 402-751, Republic of Korea.
Bioorg Med Chem. 2007 Oct 15;15(20):6535-48. doi: 10.1016/j.bmc.2007.07.010. Epub 2007 Jul 26.
A series of compounds containing one or two salicylic acid moieties were synthesized, and their efficacy to inhibit the phosphohydrolase activity of PTP1B examined. Some of the methylenedisalicylic acid derivatives were potent inhibitors of PTP1B. Of those derivatives, 3c exhibited about a 14-fold selectivity against TC-PTP, and this compound was tested in a mouse model for its efficacy to prevent diet-induced obesity. It effectively suppressed the increases in body weight and adipose mass, without any noticeable toxic effect. The compound also prevented increases in the plasma triglyceride, cholesterol, and nonesterified fatty acid concentrations; thus, expanding its therapeutic potential to other related metabolic diseases, such as hyperlipidemia and hypercholesterolemia.
合成了一系列含有一个或两个水杨酸部分的化合物,并检测了它们抑制蛋白酪氨酸磷酸酶1B(PTP1B)磷酸水解酶活性的功效。一些亚甲基二水杨酸衍生物是PTP1B的有效抑制剂。在这些衍生物中,3c对跨膜型蛋白酪氨酸磷酸酶(TC-PTP)表现出约14倍的选择性,并且在小鼠模型中测试了该化合物预防饮食诱导肥胖的功效。它有效地抑制了体重和脂肪量的增加,且没有任何明显的毒性作用。该化合物还阻止了血浆甘油三酯、胆固醇和非酯化脂肪酸浓度的升高;因此,扩大了其对其他相关代谢疾病(如高脂血症和高胆固醇血症)的治疗潜力。