生物信息学
药品
胰高血糖素样肽1受体
受体
药理学
化学
计算生物学
兴奋剂
医学
生物信息学
生物
内科学
生物化学
基因
作者
Smriti Sharma,Vinayak Bhatia
标识
DOI:10.2174/1381612826666201118094502
摘要
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.
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