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Page 1
An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus.
Lamarre D, Anderson PC, Bailey M, Beaulieu P, Bolger G, Bonneau P, Bös M, Cameron DR, Cartier M, Cordingley MG, Faucher AM, Goudreau N, Kawai SH, Kukolj G, Lagacé L, LaPlante SR, Narjes H, Poupart MA, Rancourt J, Sentjens RE, St George R, Simoneau B, Steinmann G, Thibeault D, Tsantrizos YS, Weldon SM, Yong CL, Llinàs-Brunet M. Lamarre D, et al. Among authors: cameron dr. Nature. 2003 Nov 13;426(6963):186-9. doi: 10.1038/nature02099. Epub 2003 Oct 26. Nature. 2003. PMID: 14578911 Free article. Clinical Trial.
Potent beta-lactam inhibitors of human cytomegalovirus protease.
Yoakim C, Ogilvie WW, Cameron DR, Chabot C, Grand-Maître C, Guse I, Haché B, Kawai S, Naud J, O'Meara JA, Plante R, Déziel R. Yoakim C, et al. Among authors: cameron dr. Antivir Chem Chemother. 1998 Sep;9(5):379-87. doi: 10.1177/095632029800900502. Antivir Chem Chemother. 1998. PMID: 9875391
Phosphotyrosine-containing dipeptides as high-affinity ligands for the p56lck SH2 domain.
Llinaś-Brunet M, Beaulieu PL, Cameron DR, Ferland JM, Gauthier J, Ghiro E, Gillard J, Gorys V, Poirier M, Rancourt J, Wernic D, Betageri R, Cardozo M, Jakes S, Lukas S, Patel U, Proudfoot J, Moss N. Llinaś-Brunet M, et al. Among authors: cameron dr. J Med Chem. 1999 Feb 25;42(4):722-9. doi: 10.1021/jm980612i. J Med Chem. 1999. PMID: 10052978
Optimization and determination of the absolute configuration of a series of potent inhibitors of human papillomavirus type-11 E1-E2 protein-protein interaction: a combined medicinal chemistry, NMR and computational chemistry approach.
Goudreau N, Cameron DR, Déziel R, Haché B, Jakalian A, Malenfant E, Naud J, Ogilvie WW, O'meara J, White PW, Yoakim C. Goudreau N, et al. Among authors: cameron dr. Bioorg Med Chem. 2007 Apr 1;15(7):2690-700. doi: 10.1016/j.bmc.2007.01.036. Epub 2007 Jan 24. Bioorg Med Chem. 2007. PMID: 17306550
109 results