Jahan Humera, Choudhary M Iqbal
a 1 University of Karachi, Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences , Karachi, Pakistan.
b 2 University of Karachi, H.E.J. Research Institute of Chemistry and Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences , Karachi, Pakistan (92-21) 111-222-292 ; (92-21) 99261713 ;
Expert Opin Ther Pat. 2015;25(11):1267-84. doi: 10.1517/13543776.2015.1076394. Epub 2015 Aug 17.
The glycation process, comprising a series of reactions, results in the formation of heterogeneous adducts, known as advanced glycation end products (AGEs). AGEs are involved in several pathologies, including diabetes-associated late complications, atherosclerosis, Alzheimer's disease and inflammatory arthritis. Several inhibitors of AGEs and/or reactive carbonyl species have been identified from various sources, including natural products and synthetic molecules, and have been investigated for their mechanism of action.
This review covers the literature on AGEs inhibitors published as patents between 2001 and 2014. Initially, the earlier reported molecules with AGEs inhibitory properties, their mechanism of actions and reported adverse effects are discussed. The main focus has been on the chemical structures, methods for evaluation of the activity, modes of action, pharmacokinetics and therapeutic outcomes. The potential of these AGEs inhibitors in the treatment and management of a number of diseases are also discussed in this review.
The reactive carbonyl species and AGEs have recently emerged as novel therapeutic targets for the prevention and treatment of several diseases. Currently, the major concerns with the use of AGEs inhibitors as therapeutic agents are low effectiveness, poor pharmacokinetics and undesirable side effects. Many of the AGEs inhibitors reviewed here possess potent antiglycation activity and are devoid of undesirable side effects. These small molecules inhibitors can, therefore, serve as scaffolds for the development and designing of new AGEs inhibitors as clinical agents.
糖基化过程由一系列反应组成,会导致形成异质加合物,即晚期糖基化终产物(AGEs)。AGEs参与多种病理过程,包括糖尿病相关的晚期并发症、动脉粥样硬化、阿尔茨海默病和炎性关节炎。已从包括天然产物和合成分子在内的各种来源中鉴定出几种AGEs和/或活性羰基化合物的抑制剂,并对其作用机制进行了研究。
本综述涵盖了2001年至2014年间作为专利发表的关于AGEs抑制剂的文献。首先,讨论了早期报道的具有AGEs抑制特性的分子、它们的作用机制和报道的不良反应。主要重点在于化学结构、活性评估方法、作用方式、药代动力学和治疗效果。本综述还讨论了这些AGEs抑制剂在多种疾病治疗和管理中的潜力。
活性羰基化合物和AGEs最近已成为预防和治疗多种疾病的新型治疗靶点。目前,将AGEs抑制剂用作治疗药物的主要问题是有效性低、药代动力学差和不良副作用。本文综述的许多AGEs抑制剂具有强大的抗糖基化活性,且没有不良副作用。因此,这些小分子抑制剂可作为开发和设计新型AGEs临床抑制剂的支架。