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Influenza is a highly contagious, acute upper respiratory tract disease caused by influenza virus, a member of the Orthomyxoviridae family.

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The viral particles have two surface antigens, haemagglutinin and sialidase neuraminidase that extensively decorate the surface of the virus and have been implicated in viral attachment and fusion, and the release of virion progeny, respectively. The receptor for haemagglutinin is the terminal sialic acid residue of host cell surface sialyloligosaccharides, while sialidase catalyses the hydrolysis of terminal sialic acid residues from sialyloligosaccharides.

Extensive crystallographic studies of both these proteins have revealed that the residues that interact with the sialic acid are strictly conserved.

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Therefore, these proteins make attractive targets for the design of drugs to halt the progression of the virus. Recent successful efforts in the search for new cures for influenza have led to the development of three clinically-useful anti-influenza drugs. All three are potent, selective inhibitors of influenza virus A and B sialidase.

Strategies for the development of haemagglutinin inhibitors have also been devised. Keywords: anti-influenza therapies, Influenza, influenza virus, haemagglutinin inhibitors. Abstract: Influenza is a highly contagious, acute upper respiratory tract disease caused by influenza virus, a member of the Orthomyxoviridae family.

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Neuraminidase Inhibitors as Anti-Influenza Agents. International Journal of Medicinal Chemistry , , Garry Taylor, Rupert Russell. Influenza Virus Neuraminidase Inhibitors. Palladium-catalysed allylic amination for the direct synthesis of epialkylamino-N-acetylneuraminic acid derivatives. Tetrahedron Letters , 50 , Mark von Itzstein. The war against influenza: discovery and development of sialidase inhibitors.

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When flu viruses attack! - Infectious diseases - Health & Medicine - Khan Academy

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