4.5 Review

Drug design targeting the main protease, the Achilles' heel of coronaviruses

Journal

CURRENT PHARMACEUTICAL DESIGN
Volume 12, Issue 35, Pages 4573-4590

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138161206779010369

Keywords

coronavirus; main protease; drug design

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Coronaviruses (CoVs), a genus containing about 26 known species to date, cause highly prevalent diseases and are often severe or fatal in humans and animals. In 2003, a previously unknown coronavirus was identified to be the etiological agent of a global outbreak of a form of life-threatening pneumonia called severe acute respiratory syndrome (SARS). No efficacious therapy is currently available, and vaccines and drugs are under development to prevent SARS-CoV infection in many countries. The CoV main protease (M-pro), which plays a pivotal role in viral gene expression and replication through a highly complex cascade involving the proteolytic processing of replicase polyproteins, is an attractive target for drug design. This review summarizes the recent advances in biological and structural studies, together with development of inhibitors targeting CoV M(pro)s. It is expected that inhibitors targeting CoV M(pro)s could be developed into wide-spectrum antiviral drugs against existing and possible future emerging CoV-associated diseases.

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