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Journal of Medicinal Chemistry
|
March 16, 2007
Synthesis of a new class of druglike angiotensin II C-terminal mimics with affinity for the AT2 receptor
Jennie Georgsson, Christian Sköld, Milad Botros, et al.
Journal of Medicinal Chemistry
|
November 5, 2010
Disulfide cyclized tripeptide analogues of angiotensin IV as potent and selective inhibitors of insulin-regulated aminopeptidase (IRAP)
Hanna Andersson, Heidi Demaegdt, Georges Vauquelin, et al.
Bioorganic & Medicinal Chemistry
|
October 11, 2005
Exploration of acyl sulfonamides as carboxylic acid replacements in protease inhibitors of the hepatitis C virus full-length NS3
Robert Rönn, Yogesh A Sabnis, Thomas Gossas, et al.
Journal of Medicinal Chemistry
|
December 3, 2002
Relationships between structure and interaction kinetics for HIV-1 protease inhibitors
Per-Olof Markgren, Wesley Schaal, Markku Hämäläinen, et al.
Bioorganic & Medicinal Chemistry
|
March 5, 2003
Design and synthesis of HIV-1 protease inhibitors. Novel tetrahydrofuran P2/P2'-groups interacting with Asp29/30 of the HIV-1 protease. Determination of binding from X-ray crystal structure of inhibitor protease complex
Karin Oscarsson, Martina Lahmann, Jimmy Lindberg, et al.
Bioorganic & Medicinal Chemistry
|
February 4, 2010
Discovery of potent BACE-1 inhibitors containing a new hydroxyethylene (HE) scaffold: exploration of P1' alkoxy residues and an aminoethylene (AE) central core
Catarina Björklund, Hans Adolfsson, Katarina Jansson, et al.
Chemistryopen
|
May 9, 2014
N-Aryl Isoleucine Derivatives as Angiotensin II AT2 Receptor Ligands
Malte Behrends, Charlotta Wallinder, Anna Wieckowska, et al.
Bioorganic & Medicinal Chemistry
|
August 2, 2005
Synthesis, biological evaluation, and modeling studies of inhibitors aimed at the malarial proteases plasmepsins I and II
Daniel Muthas, Daniel Nöteberg, Yogesh A Sabnis, et al.
Journal of Medicinal Chemistry
|
October 29, 2013
Design and synthesis of P1-P3 macrocyclic tertiary-alcohol-comprising HIV-1 protease inhibitors
Advait Joshi, Jean-Baptiste Véron, Johan Unge, et al.
Bioorganic & Medicinal Chemistry
|
November 5, 2002
Tetrapeptides as potent protease inhibitors of Hepatitis C Virus full-length NS3 (protease-helicase/NTPase)
Anja Johansson, Anton Poliakov, Eva Akerblom, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 109) with videos related to
Sort By:
Page
of 11
Journal of Medicinal Chemistry
|
March 16, 2007
Synthesis of a new class of druglike angiotensin II C-terminal mimics with affinity for the AT2 receptor
Jennie Georgsson, Christian Sköld, Milad Botros, et al.
Journal of Medicinal Chemistry
|
November 5, 2010
Disulfide cyclized tripeptide analogues of angiotensin IV as potent and selective inhibitors of insulin-regulated aminopeptidase (IRAP)
Hanna Andersson, Heidi Demaegdt, Georges Vauquelin, et al.
Bioorganic & Medicinal Chemistry
|
October 11, 2005
Exploration of acyl sulfonamides as carboxylic acid replacements in protease inhibitors of the hepatitis C virus full-length NS3
Robert Rönn, Yogesh A Sabnis, Thomas Gossas, et al.
Journal of Medicinal Chemistry
|
December 3, 2002
Relationships between structure and interaction kinetics for HIV-1 protease inhibitors
Per-Olof Markgren, Wesley Schaal, Markku Hämäläinen, et al.
Bioorganic & Medicinal Chemistry
|
March 5, 2003
Design and synthesis of HIV-1 protease inhibitors. Novel tetrahydrofuran P2/P2'-groups interacting with Asp29/30 of the HIV-1 protease. Determination of binding from X-ray crystal structure of inhibitor protease complex
Karin Oscarsson, Martina Lahmann, Jimmy Lindberg, et al.
Bioorganic & Medicinal Chemistry
|
February 4, 2010
Discovery of potent BACE-1 inhibitors containing a new hydroxyethylene (HE) scaffold: exploration of P1' alkoxy residues and an aminoethylene (AE) central core
Catarina Björklund, Hans Adolfsson, Katarina Jansson, et al.
Chemistryopen
|
May 9, 2014
N-Aryl Isoleucine Derivatives as Angiotensin II AT2 Receptor Ligands
Malte Behrends, Charlotta Wallinder, Anna Wieckowska, et al.
Bioorganic & Medicinal Chemistry
|
August 2, 2005
Synthesis, biological evaluation, and modeling studies of inhibitors aimed at the malarial proteases plasmepsins I and II
Daniel Muthas, Daniel Nöteberg, Yogesh A Sabnis, et al.
Journal of Medicinal Chemistry
|
October 29, 2013
Design and synthesis of P1-P3 macrocyclic tertiary-alcohol-comprising HIV-1 protease inhibitors
Advait Joshi, Jean-Baptiste Véron, Johan Unge, et al.
Bioorganic & Medicinal Chemistry
|
November 5, 2002
Tetrapeptides as potent protease inhibitors of Hepatitis C Virus full-length NS3 (protease-helicase/NTPase)
Anja Johansson, Anton Poliakov, Eva Akerblom, et al.
Page
of 11