Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, Helwan University, Helwan, Cairo 11795, Egypt.
Pharmaceutical Organic Chemistry Department, Helwan University, P.O. Box 11795, Helwan, Cairo, Egypt.
Bioorg Chem. 2022 Nov;128:106092. doi: 10.1016/j.bioorg.2022.106092. Epub 2022 Aug 10.
DPP-4Is are well recognized therapy for type 2 diabetes. In spite of sharing a common mode of action, the chemical diversity among members of DPP-4Is raised the question whether structural differences may result in distinguished activities. DPP-4Is were recently explored as drug repurposing means for treatment of SARS-CoV-2 due to the urgent need for small molecule drugs for controlling infections. The use of DPP-4Is was not correlated with adverse COVID-19-related consequences among patients with type 2 diabetes. Inspired by these reasons and the importance of pyrimidinone ring as DPP-4I with both antioxidant and anti-inflammatory activities, we succeeded to prepare some novel pyrimidinone and thio-pyrimidinone derivatives, which were then screened for their antidiabetic activity and DPP-4 inhibition. In addition, their anti-inflammatory effect on LPS-stimulated RAW 264.7 cells were evaluated. Furthermore, their antioxidant activities were also tested.
DPP-4 抑制剂是治疗 2 型糖尿病的一种公认的疗法。尽管它们具有共同的作用机制,但 DPP-4 抑制剂成员之间的化学多样性引发了一个问题,即结构差异是否会导致不同的活性。由于迫切需要小分子药物来控制感染,DPP-4 抑制剂最近被探索作为治疗 SARS-CoV-2 的药物再利用手段。在 2 型糖尿病患者中,使用 DPP-4 抑制剂与 COVID-19 相关不良后果无关。基于这些原因以及嘧啶酮环作为具有抗氧化和抗炎活性的 DPP-4I 的重要性,我们成功地制备了一些新型嘧啶酮和硫代嘧啶酮衍生物,然后对它们的抗糖尿病活性和 DPP-4 抑制作用进行了筛选。此外,还评估了它们对 LPS 刺激的 RAW 264.7 细胞的抗炎作用。此外,还测试了它们的抗氧化活性。