Synthetic and medicinal perspective of quinolines as antiviral agents

喹啉 化学 广谱 病毒 人类免疫缺陷病毒(HIV) 组合化学 登革热病毒 病毒学 药物发现 生物 有机化学 生物化学
作者
Ramandeep Kaur,Kapil Kumar
出处
期刊:European journal of medicinal chemistry [Elsevier BV]
卷期号:215: 113220-113220 被引量:194
标识
DOI:10.1016/j.ejmech.2021.113220
摘要

In current scenario, various heterocycles have come up exhibiting crucial role in various medicinal agents which are valuable for mankind. Out of diverse range of heterocycle, quinoline scaffold have been proved to play an important role in broad range of biological activities. Several drug molecules bearing a quinoline molecule with useful anticancer, antibacterial activities etc have been marketed such as chloroquine, saquinavir etc. Owing to their broad spectrum biological role, various synthetic strategies such as Skraup reaction, Combes reaction etc. has been developed by the researchers all over the world. But still the synthetic methods are associated with various limitations as formation of side products, use of expensive metal catalysts. Thus, several efforts to develop an efficient and cost effective synthetic protocol are still carried out till date. Moreover, quinoline scaffold displays remarkable antiviral activity. Therefore, in this review we have made an attempt to describe recent synthetic protocols developed by various research groups along with giving a complete explanation about the role of quinoline derivatives as antiviral agent. Quinoline derivatives were found potent against various strains of viruses like zika virus, enterovirus, herpes virus, human immunodeficiency virus, ebola virus, hepatitis C virus, SARS virus and MERS virus etc.
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