Influenza virus fluAH1N1 still remains a target for its inhibition with smallmolecules. Fleeting nitrosocarbonyl intermediates are at work in a short-cut synthesis of carbocyclic nucleoside analogues. The strategy of the synthetic approaches is presented along with the in vitro antiviral tests.The nucleoside derivatives were tested for their inhibitory activity against a variety of viruses. Promising antiviral activities were found for specific compounds in the case of flu A H1N1
The investigation of brand new compounds with potential anti-viral activity is currently in the lime...
[Figure not available: see fulltext.] The minireview surveys the modification of native nucleosides ...
Influenza viruses are responsible for seasonal epidemics and occasional pandemics which cause signif...
Influenza virus fluAH1N1 still remains a target for its inhibition with smallmolecules. Fleeting nit...
Copyright © 2014 Dalya Al-Saad et al. This is an open access article distributed under the Creative ...
The synthesis of isoxazolino-carbocyclic nornucleosides incorporating a quinoline moiety was tuned ...
Isoxazolino-carbocyclic anthracene nor-nucleosides were prepared through nitrosocarbonyl chemistry ...
Les analogues nucléosidiques constituent une famille importante d'agents thérapeutiques dans le trai...
The SARS-CoV-2 betacoronavirus pandemic has claimed more than 6.5 million lives and, despite the dev...
A new adenine derivative is prepared through the chemistry of nitrosocarbonyl intermediates. The sy...
The influenza virus neuraminidase (NA) is essential for viral infection and offers a potential targe...
A set of 20 nucleoside analogs were examined for their inhibitory effects on the cytopathogenicity a...
Enantiomerically pure cyclopentyl cytosine [(−)-carbodine 1] was synthesized from d-ribose and evalu...
Enantiomerically pure cyclopentyl cytosine [(−)-carbodine 1] was synthesized from d-ribose and evalu...
The development of new nucleoside analogues as antiviral agents has remained an attractive research ...
The investigation of brand new compounds with potential anti-viral activity is currently in the lime...
[Figure not available: see fulltext.] The minireview surveys the modification of native nucleosides ...
Influenza viruses are responsible for seasonal epidemics and occasional pandemics which cause signif...
Influenza virus fluAH1N1 still remains a target for its inhibition with smallmolecules. Fleeting nit...
Copyright © 2014 Dalya Al-Saad et al. This is an open access article distributed under the Creative ...
The synthesis of isoxazolino-carbocyclic nornucleosides incorporating a quinoline moiety was tuned ...
Isoxazolino-carbocyclic anthracene nor-nucleosides were prepared through nitrosocarbonyl chemistry ...
Les analogues nucléosidiques constituent une famille importante d'agents thérapeutiques dans le trai...
The SARS-CoV-2 betacoronavirus pandemic has claimed more than 6.5 million lives and, despite the dev...
A new adenine derivative is prepared through the chemistry of nitrosocarbonyl intermediates. The sy...
The influenza virus neuraminidase (NA) is essential for viral infection and offers a potential targe...
A set of 20 nucleoside analogs were examined for their inhibitory effects on the cytopathogenicity a...
Enantiomerically pure cyclopentyl cytosine [(−)-carbodine 1] was synthesized from d-ribose and evalu...
Enantiomerically pure cyclopentyl cytosine [(−)-carbodine 1] was synthesized from d-ribose and evalu...
The development of new nucleoside analogues as antiviral agents has remained an attractive research ...
The investigation of brand new compounds with potential anti-viral activity is currently in the lime...
[Figure not available: see fulltext.] The minireview surveys the modification of native nucleosides ...
Influenza viruses are responsible for seasonal epidemics and occasional pandemics which cause signif...