Could 5'-N and S ProTide analogues work as prodrugs of antiviral agents?
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31882298
DOI
10.1016/j.bmcl.2019.126897
PII: S0960-894X(19)30875-3
Knihovny.cz E-zdroje
- Klíčová slova
- (31)P NMR spectroscopy, Antiviral, HCV, Nucleotide, ProTide, Prodrug,
- MeSH
- adenosin analogy a deriváty chemie MeSH
- antivirové látky chemická syntéza chemie farmakologie MeSH
- dusík chemie MeSH
- Hepacivirus účinky léků MeSH
- lidé MeSH
- magnetická rezonanční spektroskopie MeSH
- nukleotidy chemie metabolismus farmakologie MeSH
- prekurzory léčiv chemická syntéza chemie farmakologie MeSH
- síra chemie MeSH
- virus dengue účinky léků MeSH
- virus zika účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2-methyladenosine MeSH Prohlížeč
- adenosin MeSH
- antivirové látky MeSH
- dusík MeSH
- nukleotidy MeSH
- prekurzory léčiv MeSH
- síra MeSH
The nucleoside/nucleotide derived antiviral agents have been the most important components of antiviral therapy used in clinics. Recently, the focus of the medicinal chemists within this exciting research field has been affected mainly by the lack of effective therapies for the Hepatitis C virus (HCV) infection and several other "neglected" diseases caused by viruses such as Zika or Dengue. 2'-Methyl modified nucleosides and their monophosphate prodrugs (ProTides) have revolutionized the therapies for HCV in the last few years and, according to the latest research efforts, have also brought a promise for treatment of diseases caused by other members of Flaviviridae family. Here, we report on the design and synthesis of 5'-N and S modified ProTides derived from 2'-methyladenosine. We studied potential applicability of these derivatives as prodrugs of this archetypal antiviral compound.
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