Department of Chemistry, Miranda House, University of Delhi, Delhi, India.
ICARE Eye Hospital and Postgraduate Institute, U.P., Noida, India.
Curr Pharm Des. 2021;27(8):1015-1024. doi: 10.2174/1381612826666201118094502.
Drug design based on degradation-resistant, long-acting Glucagon-like peptide-1 receptor (GLP-1R) agonists for treating type 2 diabetes is attracting a lot of attention. Here, the authors have examined in detail how in silico drug design is aiding in developing novel GLP-1 receptor agonist drugs. Their pharmacotherapy and adverse effects have also been summarized. After the analysis of currently available information on this topic, the authors feel that in silico method is a great auxiliary tool in almost all the experimental studies on GLP-1 receptors and is highly efficient in identifying novel drug molecules that can act as GLP-1 receptor agonists.
基于不易降解、长效的胰高血糖素样肽-1 受体 (GLP-1R) 激动剂的药物设计,用于治疗 2 型糖尿病,正受到广泛关注。本文作者详细探讨了计算机辅助药物设计如何帮助开发新型 GLP-1 受体激动剂药物,并对其药物治疗和不良反应进行了总结。在分析了该主题的现有信息后,作者认为,在计算机辅助药物设计几乎所有关于 GLP-1 受体的实验研究中都是一种很好的辅助工具,它在识别可作为 GLP-1 受体激动剂的新型药物分子方面非常高效。