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ScientificWorldJournal ; 2014: 472373, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25610906

RESUMO

Influenza virus flu A H1N1 still remains a target for its inhibition with small molecules. 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.


Assuntos
Antivirais/síntese química , Cicloexanóis/síntese química , Vírus da Influenza A Subtipo H1N1/efeitos dos fármacos , Quinolinas/síntese química , Antivirais/farmacologia , Cicloexanóis/farmacologia , Quinolinas/farmacologia
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