Fine tuning of PPAR ligands for type 2 diabetes and metabolic syndrome

被引:41
|
作者
Ramachandran, U [1 ]
Kumar, R [1 ]
Mittal, A [1 ]
机构
[1] NIPER, Dept Pharmaceut Technol, Sector 67, SAS Nagar 160062, Punjab, India
关键词
T2DM; PPAR; TZDs; dual agonist; pan agonist; partial agonist;
D O I
10.2174/138955706776876140
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Type 2 diabetes mellitus (T2DM) is highly prevalent chronic disease. Recently, many biological targets are discovered for treatment of this disease. The identification of the nuclear hormone receptor peroxisome proliferator activated receptors (PPAR) and their subtypes alpha, gamma and delta or beta as targets for controlling lipid, glucose and energy homeostasis has proved to be exciting. As hyperlipidaemia, obesity and insulin resistance are independent risk factors for coronary heart disease and macrovascular complications of diabetes; new agents that increase insulin sensitivity as well as decrease hyperlipidaemia by distinct yet complementary mechanism are being studied as they may provide improved therapy for T2DM and related disorders. In this article, we review highly potent PPAR gamma agonists, PPAR alpha/gamma dual agonists, PPAR pan agonists, alternative PPAR ligands like partial agonists or selective PPAR modulators (SPPARMs) and antagonists from a chemist point of view.
引用
收藏
页码:563 / 573
页数:11
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