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Dale R. Cameron

Boehringer Ingelheim

31

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1725

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Crystal Structure of the E2 Transactivation Domain of Human Papillomavirus Type 11 Bound to a Protein Interaction Inhibitor

2004 Journal of Biological Chemistry
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Potent Inhibitors of the Hepatitis C Virus NS3 Protease: Design and Synthesis of Macrocyclic Substrate-Based [beta]-Strand Mimics

2004 Journal of Organic Chemistry
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Potent Inhibitors of the Hepatitis C Virus NS3 Protease: Design and Synthesis of Macrocyclic Substrate-Based β-Strand Mimics.

2004 ChemInform
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Peptide-based inhibitors of the hepatitis C virus NS3 protease: structure-activity relationship at the C-terminal position.

2004 Journal of Medicinal Chemistry
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NMR structural characterization of peptide inhibitors bound to the Hepatitis C virus NS3 protease: design of a new P2 substituent.

2004 Journal of Medicinal Chemistry
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Corrigendum: An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus

2004 Nature
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An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus

2003 Nature
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Design and Synthesis of Macrocyclic Inhibitors of the Hepatitis C NS3 Protease

2003
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Macrocyclic Inhibitors of the NS3 Protease as Potential Therapeutic Agents of Hepatitis C Virus Infection

2003 Angewandte Chemie
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Cocrystallization e2 transactivation domain of human papilloma / inhibitor and x-ray coordinates that define the binding pocket inhibitor virus.

2002
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