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Bioorganic & Medicinal Chemistry|October 11, 2005
Exploration of acyl sulfonamides as carboxylic acid replacements in protease inhibitors of the hepatitis C virus full-length NS3Robert Rönn, Yogesh A Sabnis, Thomas Gossas, et al.
Bioorganic & Medicinal Chemistry|April 24, 2007
Evaluation of a diverse set of potential P1 carboxylic acid bioisosteres in hepatitis C virus NS3 protease inhibitorsRobert Rönn, Thomas Gossas, Yogesh A Sabnis, et al.
Bioorganic & Medicinal Chemistry|January 16, 2008
Hepatitis C virus NS3 protease inhibitors comprising a novel aromatic P1 moietyRobert Rönn, Anna Lampa, Shane D Peterson, et al.
Bioorganic & Medicinal Chemistry|November 23, 2006
Phenylglycine as a novel P2 scaffold in hepatitis C virus NS3 protease inhibitorsPernilla Ortqvist, Shane D Peterson, Eva Kerblom, et al.
Biochemistry|August 7, 2010
Effect of the protonation state of the titratable residues on the inhibitor affinity to BACE-1José L Domínguez, Tony Christopeit, M Carmen Villaverde, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2015
Molecular blueprint of allosteric binding sites in a homologue of the agonist-binding domain of the α7 nicotinic acetylcholine receptorRadovan Spurny, Sarah Debaveye, Ana Farinha, et al.
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