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新型吡咯并嘧啶衍生物的设计、合成、分子对接、分子模拟及抗氧化和抗炎活性评价。

Novel pyrrolopyrimidine derivatives: design, synthesis, molecular docking, molecular simulations and biological evaluations as antioxidant and anti-inflammatory agents.

机构信息

Pharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Helwan University, Cairo, Egypt.

Biochemistry Department, Faculty of Agriculture, Cairo University, Cairo, Egypt.

出版信息

J Enzyme Inhib Med Chem. 2022 Dec;37(1):1821-1837. doi: 10.1080/14756366.2022.2090546.

Abstract

Current medical approaches to control the Covid-19 pandemic are either to directly target the SARS-CoV-2 innovate a defined drug and a safe vaccine or indirectly target the medical complications of the virus. One of the indirect strategies for fighting this virus has been mainly dependent on using anti-inflammatory drugs to control cytokines storm responsible for severe health complications. We revealed the discovery of novel fused pyrrolopyrimidine derivatives as promising antioxidant and anti-inflammatory agents. The newly synthesised compounds were evaluated for their in vitro anti-inflammatory activity using RAW264.7 cells after stimulation with lipopolysaccharides (LPS). The results revealed that and were the most potent analogues. Molecular docking and simulations of these compounds against COX-2, TLR-2 and TLR-4 respectively was performed. The former results were in line with the biological data and proved that and have potential antioxidant and anti-inflammatory effects.

摘要

目前控制新冠疫情的医学方法,或是直接针对 SARS-CoV-2 研发特效药和安全疫苗,或是间接针对病毒引发的医疗并发症。对抗该病毒的间接策略之一,主要依赖于使用抗炎药物来控制细胞因子风暴,以应对严重的健康并发症。我们发现了新型融合吡咯嘧啶衍生物,它们具有成为有前途的抗氧化和抗炎药物的潜力。新合成的化合物在脂多糖 (LPS) 刺激 RAW264.7 细胞后,用于评估其体外抗炎活性。结果表明 和 是最有效的类似物。对这些化合物进行了针对 COX-2、TLR-2 和 TLR-4 的分子对接和模拟。前者的结果与生物学数据一致,证明 和 具有潜在的抗氧化和抗炎作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf4f/9246196/8c86cfab2540/IENZ_A_2090546_UF0001_C.jpg

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