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Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of unsymmetrical 1-hydroxy-4,4-dialkyl-3-oxo-3,4-dihydronaphthalene benzothiadiazine derivatives
Authors:Krueger A Chris  Madigan Darold L  Green Brian E  Hutchinson Douglas K  Jiang Wen W  Kati Warren M  Liu Yaya  Maring Clarence J  Masse Sherie V  McDaniel Keith F  Middleton Tim R  Mo Hongmei  Molla Akhteruzzaman  Montgomery Debra A  Ng Teresa I  Kempf Dale J
Institution:Infectious Disease Research, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL 60064, USA. a.chris.krueger@abbott.com
Abstract:Substituted 1-hydroxy-4,4-dialkyl-3-oxo-3,4-dihydronaphthalene benzothiadiazine derivatives were investigated as inhibitors of genotype 1 HCV polymerase. Structure-activity relationship patterns for this class of compounds are discussed. It was found that the saturated alkane dialkyl units provided the most active analogs.
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