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Acta Pharmaceutica Sinica ; (12): 289-299, 2010.
Article Dans Chinois | WPRIM | ID: wpr-250589

Résumé

Influenza is a major threat to millions of people worldwide. Vaccines and antiviral agents are two main options available to reduce the impact of the influenza virus, while anti-influenza agents are the most effective means to prevent the transmission of the highly contagious virus and to treat the epidemics of disease. At present, four anti-influenza agents have been approved by the FDA for the treatment of influenza, including two M2 protein ion channel inhibitors-amantadine and rimantadine and two neuraminidase inhibitors-zanamivir and oseltamivir. Arbidol hydrochloride, launched in Russia, is a potent inhibitor of influenza virus, too. Neuraminidase inhibitors could be classified generally by structure into six different kinds: sialic acid derivatives, benzoic acid derivatives, cyclohexene derivatives, cyclopentane derivatives, pyrrolidine derivatives and natural products. In this paper, recent progress in the research of the action mechanisms and structure-activity relationships of these anti-influenza virus agents were reviewed.


Sujets)
Humains , Amantadine , Chimie , Pharmacologie , Utilisations thérapeutiques , Antiviraux , Chimie , Pharmacologie , Utilisations thérapeutiques , Cyclopentanes , Chimie , Pharmacologie , Utilisations thérapeutiques , Guanidines , Chimie , Pharmacologie , Utilisations thérapeutiques , Indoles , Chimie , Pharmacologie , Utilisations thérapeutiques , Grippe humaine , Traitement médicamenteux , Sialidase , Chimie , Pharmacologie , Utilisations thérapeutiques , Orthomyxoviridae , Oséltamivir , Chimie , Pharmacologie , Utilisations thérapeutiques , Pyrrolidines , Chimie , Pharmacologie , Utilisations thérapeutiques , Rimantadine , Chimie , Pharmacologie , Utilisations thérapeutiques , Relation structure-activité , Protéines de la matrice virale , Chimie , Pharmacologie , Utilisations thérapeutiques , Zanamivir , Chimie , Pharmacologie , Utilisations thérapeutiques
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