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Postgraduate Medical Journal 2005;81:71-78
© 2005 Fellowship of Postgraduate Medicine


REVIEW

Artemisinins

C J Woodrow 1, R K Haynes 2, S Krishna 1

1 Department of Cellular and Molecular Medicine, Infectious Diseases, St George’s Hospital Medical School, Tooting, London, UK
2 Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong

Correspondence to:
Correspondence to:
Professor S Krishna
Department of Cellular and Molecular Medicine, Infectious Diseases, St George’s Hospital Medical School, Cranmer Terrace, Tooting, London SW17 0RE, UK; s.krishna{at}sghms.ac.uk

Artemisinins were discovered to be highly effective antimalarial drugs shortly after the isolation of the parent artemisinin in 1971 in China. These compounds combine potent, rapid antimalarial activity with a wide therapeutic index and an absence of clinically important resistance. Artemisinin containing regimens meet the urgent need to find effective treatments for multidrug resistant malaria and have recently been advocated for widespread deployment. Comparative trials of artesunate and quinine for severe malaria are in progress to see if the persistently high mortality of this condition can be reduced.


Keywords: artemisinin; qinghaosu; malaria; multidrug resistant; PfATPase6




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