Discovery of Novel PTP1B Inhibitors by High-throughput Virtual Screening

广告 虚拟筛选 药物发现 胰岛素受体 对接(动物) 2型糖尿病 药品 计算生物学 胰岛素抵抗 葡萄糖稳态 胰岛素 高通量筛选 药理学 糖尿病 生物 生物信息学 医学 生物技术 内分泌学 护理部
作者
Abhijit Debnath,Anjna Rani,Rupa Mazumder,Avijit Mazumder,Rajesh Kumar Singh,Shalini Sharma,Shikha Srivastava,Hema Chaudhary,Rashmi Mishra,Navneet Khurana,Jahanvi Sanchitra,Sk Ashif Jan
出处
期刊:Current Computer - Aided Drug Design [Bentham Science Publishers]
卷期号:21 被引量:3
标识
DOI:10.2174/0115734099278007241004105500
摘要

Aim: To Discover novel PTP1B inhibitors by high-throughput virtual screening Background: Type 2 Diabetes is a significant global health concern. According to projections, the estimated number of individuals affected by the condition will reach 578 million by the year 2030 and is expected to further increase to 700 million deaths by 2045. Protein Tyrosine Phosphatase 1B is an enzymatic protein that has a negative regulatory effect on the pathways involved in insulin signaling. This regulatory action ultimately results in the development of insulin resistance and the subsequent elevation of glucose levels in the bloodstream. The proper functioning of insulin signaling is essential for maintaining glucose homeostasis, whereas the disruption of insulin signaling can result in the development of type 2 diabetes. Consequently, we sought to utilize PTP1B as a drug target in this investigation. Objective: The purpose of our study was to identify novel PTP1B inhibitors as a potential treatment for managing type 2 diabetes. Methods: To discover potent PTP1B inhibitors, we have screened the Maybridge HitDiscover database by SBVS. Top hits have been passed based on various drug-likeness rules, toxicity predictions, ADME assessment, Consensus Molecular docking, DFT, and 300 ns MD Simulations. Results: Two compounds have been identified with strong binding affinity at the active site of PTP1B along with drug-like properties, efficient ADME, low toxicity, and high stability. Conclusion: The identified molecules could potentially manage T2DM effectively by inhibiting PTP1B, providing a promising avenue for therapeutic strategies.
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