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喹啉作为抗病毒药物的合成及药用前景。

Synthetic and medicinal perspective of quinolines as antiviral agents.

作者信息

Kaur Ramandeep, Kumar Kapil

机构信息

Department of Pharmaceutical Chemistry, Indo-Soviet Friendship College of Pharmacy (ISFCP), Moga, Punjab, 142001, India.

School of Pharmacy and Technology Management, SVKM's NMIMS, Hyderabad, Telangana, 509301, India.

出版信息

Eur J Med Chem. 2021 Apr 5;215:113220. doi: 10.1016/j.ejmech.2021.113220. Epub 2021 Jan 24.

Abstract

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.

摘要

在当前情况下,各种杂环化合物在对人类有价值的各种药物制剂中发挥着关键作用。在各种各样的杂环化合物中,喹啉骨架已被证明在广泛的生物活性中起重要作用。一些带有喹啉分子且具有有用的抗癌、抗菌活性等的药物分子已上市,如氯喹、沙奎那韦等。由于其广泛的生物作用,世界各地的研究人员已开发出各种合成策略,如斯克劳普反应、康布斯反应等。但这些合成方法仍存在各种局限性,如副产物的形成、使用昂贵的金属催化剂。因此,迄今为止仍在进行多项努力以开发一种高效且经济有效的合成方案。此外,喹啉骨架显示出显著的抗病毒活性。因此,在本综述中,我们试图描述各个研究小组最近开发的合成方案,并对喹啉衍生物作为抗病毒剂的作用给出完整解释。已发现喹啉衍生物对多种病毒株有效,如寨卡病毒、肠道病毒、疱疹病毒、人类免疫缺陷病毒、埃博拉病毒、丙型肝炎病毒、非典病毒和中东呼吸综合征病毒等。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6915/7995244/ef2aec80493f/fx1_lrg.jpg

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