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Nils Gunnar Johansson

University of Texas at Austin

47

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Discovery and Optimizationof a Compound Series Activeagainst Trypanosoma cruzi, the Causative Agent ofChagas Disease

2020 Journal of Medicinal Chemistry
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Validation of Plasmodium falciparum dUTPase as the target of 5′-tritylated deoxyuridine analogues with anti-malarial activity

2019 Malaria Journal
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Investigation of acyclic uridine amide and 5′-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase

2013 Bioorganic & Medicinal Chemistry
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Discovery of 4′-azido-2′-deoxy-2′-C-methyl cytidine and prodrugs thereof: A potent inhibitor of Hepatitis C virus replication

2012 Bioorganic & Medicinal Chemistry Letters
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A potent inhibitor of Hepatitis C virus replication

2012
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β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase

2011 Bioorganic & Medicinal Chemistry
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Catalytic Osmylation and Antiviral Activity of Some Carbocyclic 5- Substituted Uridine and Cytidine Analogues.

2010 ChemInform
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The design, synthesis, and antiviral activity of monofluoro and difluoro analogues of 4'-azidocytidine against hepatitis C virus replication: the discovery of 4'-azido-2'-deoxy-2'-fluorocytidine and 4'-azido-2'-dideoxy-2',2'-difluorocytidine.

2009 Journal of Medicinal Chemistry
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2′-Deoxy-nucleoside Analogs can be Potent Dual Inhibitors of HCV and HIV Replication with Selectivity against Human Polymerases

2009 Antiviral Research
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952 2′ -DEOXY-NUCLEOSIDE ANALOGS AS POTENT DUAL INHIBITORS OF HCV AND HIV REPLICATION, WITH SELECTIVITY AGAINST OTHER VIRAL AND HUMAN POLYMERASES

2009 Journal of Hepatology
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