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Expert Opinion on Therapeutic Targets
|
January 24, 2003
Targeting HIV-1 integrase
Khampoune Sayasith, Gilles Sauvé, Jocelyn Yelle
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2005
Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure-activity relationship studies
Abderrahim Bouzide, Gilles Sauvé, Jocelyn Yelle
Bioorganic & Medicinal Chemistry Letters
|
September 25, 2003
1,2,5,6-tetra-O-benzyl-D-mannitol derivatives as novel HIV protease inhibitors
Abderrahim Bouzide, Gilles Sauvé, Guy Sévigny, et al.
AAPS Pharmsci
|
July 10, 2002
Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?
Carole Lavigne, Jocelyn Yelle, Gilles Sauve, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2003
Lysine sulfonamides as novel HIV-protease inhibitors: optimization of the Nepsilon-acyl-phenyl spacer
Brent R Stranix, Gilles Sauvé, Abderrahim Bouzide, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 1, 2004
Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas
Brent R Stranix, Gilles Sauvé, Abderrahim Bouzide, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 29, 2006
Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-acyl aromatic alpha-amino acids
Brent R Stranix, Jean-François Lavallée, Guy Sévigny, et al.
Antimicrobial Agents and Chemotherapy
|
July 20, 2007
In vitro antiviral activity and cross-resistance profile of PL-100, a novel protease inhibitor of human immunodeficiency virus type 1
Serge Dandache, Guy Sévigny, Jocelyn Yelle, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Expert Opinion on Therapeutic Targets
|
January 24, 2003
Targeting HIV-1 integrase
Khampoune Sayasith, Gilles Sauvé, Jocelyn Yelle
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2005
Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure-activity relationship studies
Abderrahim Bouzide, Gilles Sauvé, Jocelyn Yelle
Bioorganic & Medicinal Chemistry Letters
|
September 25, 2003
1,2,5,6-tetra-O-benzyl-D-mannitol derivatives as novel HIV protease inhibitors
Abderrahim Bouzide, Gilles Sauvé, Guy Sévigny, et al.
AAPS Pharmsci
|
July 10, 2002
Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?
Carole Lavigne, Jocelyn Yelle, Gilles Sauve, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2003
Lysine sulfonamides as novel HIV-protease inhibitors: optimization of the Nepsilon-acyl-phenyl spacer
Brent R Stranix, Gilles Sauvé, Abderrahim Bouzide, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 1, 2004
Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas
Brent R Stranix, Gilles Sauvé, Abderrahim Bouzide, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 29, 2006
Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-acyl aromatic alpha-amino acids
Brent R Stranix, Jean-François Lavallée, Guy Sévigny, et al.
Antimicrobial Agents and Chemotherapy
|
July 20, 2007
In vitro antiviral activity and cross-resistance profile of PL-100, a novel protease inhibitor of human immunodeficiency virus type 1
Serge Dandache, Guy Sévigny, Jocelyn Yelle, et al.
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of 1