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Neuraminidases, rational drug design

Rational drug design led to the design of new inhibitors of neuraminidase—an enzyme important to replication of influenza virus.280 The... [Pg.41]

The most studied sialidase is the influenza virus neuraminidase, whose structure was reported over 15 years ago [9], and which has been the target of highly successful rational drug design [10-12]. Influenza type A and B viruses have two surface proteins, hemagglutinin (HA) which attaches the virus to host cells by recognizing sialic... [Pg.1597]

See other pages where Neuraminidases, rational drug design is mentioned: [Pg.7]    [Pg.12]    [Pg.97]    [Pg.278]    [Pg.646]    [Pg.159]    [Pg.161]    [Pg.153]    [Pg.13]    [Pg.158]    [Pg.609]    [Pg.139]    [Pg.609]    [Pg.480]    [Pg.3008]    [Pg.1935]    [Pg.561]    [Pg.403]    [Pg.318]   
See also in sourсe #XX -- [ Pg.741 ]



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Drug rational

Neuraminidase

Neuraminidases

Rational

Rational design

Rationalism

Rationally designed drug

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