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Antimicrobial Agents and Chemotherapy, September 2008, p. 3433-3437, Vol. 52, No. 9
0066-4804/08/$08.00+0 doi:10.1128/AAC.01534-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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Rega Institute for Medical Research, K.U. Leuven, 3000 Leuven, Belgium,1 Department of Pharmaceutical Chemistry, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria,2 Dipartimento di Chimica e Tecnologia del Farmaco, Università degli Studi di Perugia, Perugia, Italy,3 Department of Molecular Virology, University of Heidelberg, 69120 Heidelberg, Germany4
Received 28 November 2007/ Returned for modification 16 January 2008/ Accepted 8 July 2008
We report here a comparative study of the anti-hepatitis C virus (HCV) activities of selected (i) nucleoside polymerase, (ii) nonnucleoside polymerase, (iii)
,
-diketo acid polymerase, (iv) NS3 protease, and (v) helicase inhibitors, as well as (vi) cyclophilin binding molecules and (vii) alpha 2b interferon in four different HCV genotype 1b replicon systems.
Published ahead of print on 14 July 2008.
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