Mahal Ahmed, Duan Meitao, Zinad Dhafer S, Mohapatra Ranjan K, Obaidullah Ahmad J, Wei Xiaoyi, Pradhan Manoj K, Das Debadutta, Kandi Venkataramana, Zinad Hany S, Zhu Quanhong
Department of Medical Biochemical Analysis, College of Health Technology, Cihan University-Erbil Erbil Kurdistan Region Iraq
Key Laboratory of Plant Resources Conservation and Sustainable Utilization, Guangdong Provincial Key Laboratory of Applied Botany, Chinese Academy of Sciences South China Botanical Garden Guangzhou 510650 People's Republic of China.
RSC Adv. 2021 Jan 6;11(3):1804-1840. doi: 10.1039/d0ra07283d. eCollection 2021 Jan 4.
Influenza virus is the main cause of an infectious disease called influenza affecting the respiratory system including the throat, nose and lungs. Neuraminidase inhibitors are reagents used to block the enzyme called neuraminidase to prevent the influenza infection from spreading. Neuraminidase inhibitors are widely used in the treatment of influenza infection, but still there is a need to develop more potent agents for the more effective treatment of influenza. Complications of the influenza disease lead to death, and one of these complications is drug resistance; hence, there is an urgent need to develop more effective agents. This review focuses on the recent advances in chemical synthesis pathways used for the development of new neuraminidase agents along with the medicinal aspects of chemically modified molecules, including the structure-activity relationship, which provides further rational designs of more active small molecules.
流感病毒是一种名为流感的传染病的主要病因,该疾病会影响包括咽喉、鼻子和肺部在内的呼吸系统。神经氨酸酶抑制剂是用于阻断名为神经氨酸酶的酶,以防止流感感染扩散的试剂。神经氨酸酶抑制剂被广泛用于治疗流感感染,但仍需要开发更有效的药物来更有效地治疗流感。流感疾病的并发症会导致死亡,其中一种并发症就是耐药性;因此,迫切需要开发更有效的药物。这篇综述聚焦于用于开发新型神经氨酸酶药物的化学合成途径的最新进展,以及化学修饰分子的药学方面,包括构效关系,这为更具活性的小分子提供了进一步的合理设计。