scholarly journals Advances in antiviral nucleoside analogues and their prodrugs

2018 ◽  
Vol 26 ◽  
pp. 204020661878141 ◽  
Author(s):  
Katherine Seley-Radtke ◽  
Jerome Deval
Viruses ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 667
Author(s):  
Robert J. Geraghty ◽  
Matthew T. Aliota ◽  
Laurent F. Bonnac

The emergence or re-emergence of viruses with epidemic and/or pandemic potential, such as Ebola, Zika, Middle East Respiratory Syndrome (MERS-CoV), Severe Acute Respiratory Syndrome Coronavirus 1 and 2 (SARS and SARS-CoV-2) viruses, or new strains of influenza represents significant human health threats due to the absence of available treatments. Vaccines represent a key answer to control these viruses. However, in the case of a public health emergency, vaccine development, safety, and partial efficacy concerns may hinder their prompt deployment. Thus, developing broad-spectrum antiviral molecules for a fast response is essential to face an outbreak crisis as well as for bioweapon countermeasures. So far, broad-spectrum antivirals include two main categories: the family of drugs targeting the host-cell machinery essential for virus infection and replication, and the family of drugs directly targeting viruses. Among the molecules directly targeting viruses, nucleoside analogues form an essential class of broad-spectrum antiviral drugs. In this review, we will discuss the interest for broad-spectrum antiviral strategies and their limitations, with an emphasis on virus-targeted, broad-spectrum, antiviral nucleoside analogues and their mechanisms of action.


Author(s):  
Mauro Magnani ◽  
Luigia Rossi ◽  
Anna Casabianca ◽  
Alessandra Fraternale ◽  
Giuditta Schiavano ◽  
...  

1990 ◽  
Vol 55 (s1) ◽  
pp. 17-20 ◽  
Author(s):  
Mikko Oivanen ◽  
Tuula Viinamäki ◽  
Sergei Zavgorodny ◽  
Michael Polianski ◽  
Alex Azhayev ◽  
...  

2009 ◽  
Vol 20 (1) ◽  
pp. 37-46 ◽  
Author(s):  
Zhimeng Wu ◽  
John C Drach ◽  
Mark N Prichard ◽  
Milka Yanachkova ◽  
Ivan Yanachkov ◽  
...  

Background: Following the example of L-valine prodrugs of antiviral nucleoside analogues, L-valine ester of cyclopropavir (valcyclopropavir) was synthesized. Methods: The known tetrahydropyranylcyclopropavir was transformed to N-( tert-butoxycarbonyl)-L-valine ester, which was deprotected to valcyclopropavir. Results: Stability of valcyclopropavir towards hydrolysis at pH 7.0 roughly corresponded to that of valganciclovir. Valcyclopropavir inhibited replication of human cytomegalovirus (HCMV, Towne and AD169 strains) to approximately the same extent as the parent drug cyclopropavir. Pharmacokinetic studies in mice established that the oral bioavailability of valcyclopropavir was 95%. Conclusions: The prodrug valcyclopropavir offers some improved therapeutic parameters over the parent compound cyclopropavir.


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