A comprehensive update on the structure and synthesis of potential drug targets for combating the coronavirus pandemic caused by SARS-CoV-2

被引:3
|
作者
Malik, Prerna [1 ]
Jain, Sonika [1 ]
Jain, Pankaj [2 ]
Kumawat, Jyoti [1 ]
Dwivedi, Jaya [1 ]
Kishore, Dharma [1 ]
机构
[1] Banasthali Vidyapith, Dept Chem, Jaipur 304022, Rajasthan, India
[2] Banasthali Vidyapith, Dept Pharm, Jaipur, Rajasthan, India
关键词
COVID-19; pandemic; Delta plus variant; lopinavir; remdesivir; SARS-CoV-2; variant; PROTEASE INHIBITOR; ANTIVIRAL ACTIVITY; FLUORINATED NUCLEOSIDES; FAVIPIRAVIR T-705; EBOLA-VIRUS; EFFICACY; DESIGN; GEMCITABINE; CHLOROQUINE; COVID-19;
D O I
10.1002/ardp.202100382
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The outbreak of the coronavirus pandemic COVID-19 created by its severe acute respiratory syndrome corona virus-2 (SARS-CoV-2) variant, known for producing a very severe acute respiratory syndrome, has created an unprecedented situation by its continual assault around the world. The crisis caused by the SARS-CoV-2 variant has been a global challenge, calling to mitigate this unprecedented pandemic that has engulfed the whole world. Since the outbreak and spread of COVID-19, many researchers globally have been grappling to find new clinically trialed active drugs with anti-COVID-19 activity, from antimalarial drugs to JAK inhibitors, antiviral drugs, immune suppressants, and so forth. This article presents a brief discussion on the activity and synthesis of some active molecules such as favipiravir, hydroxychloroquine, pirfenidone, remdesivir, lopinavir, camostat, chloroquine, baricitinib, molnupiravir, and so forth, which are under trial.
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页数:27
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