Abstract
Structure-based drug design, a terminology used to describe rational drug design by complementing the structure, spatially and chemically, of the target macromolecule, is rapidly developing as one of the innovative approaches to drug discovery. A growing volume of protein structure data and new techniques of protein structure determination make this all possible. The method of structure-based drug design and a specific example of the design of influenza virus neuraminidase is briefly presented. A whole new class of influenza virus neuraminidase inhibitors has been designed that can potentially be developed as antiinfluenza drugs.
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CITATION STYLE
Luo, M., Air, G. M., & Brouillette, W. J. (1997). Design of aromatic inhibitors of influenza virus neuraminidase. In Journal of Infectious Diseases (Vol. 176). Oxford University Press. https://doi.org/10.1086/514178
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