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Journal of Medicinal Chemistry
|
March 3, 2006
Microwave-accelerated synthesis of P1'-extended HIV-1 protease inhibitors encompassing a tertiary alcohol in the transition-state mimicking scaffold
Jenny K Ekegren, Nina Ginman, Asa Johansson, et al.
Journal of Medicinal Chemistry
|
April 12, 2011
Potent macrocyclic inhibitors of insulin-regulated aminopeptidase (IRAP) by olefin ring-closing metathesis
Hanna Andersson, Heidi Demaegdt, Anders Johnsson, et al.
Plos One
|
April 23, 2014
Direct angiotensin AT2 receptor stimulation using a novel AT2 receptor agonist, compound 21, evokes neuroprotection in conscious hypertensive rats
Claudia A McCarthy, Antony Vinh, Alyson A Miller, et al.
Bioorganic & Medicinal Chemistry
|
November 17, 2006
Synthesis of novel potent hepatitis C virus NS3 protease inhibitors: discovery of 4-hydroxy-cyclopent-2-ene-1,2-dicarboxylic acid as a N-acyl-L-hydroxyproline bioisostere
Fredrik Thorstensson, Fredrik Wångsell, Ingemar Kvarnström, et al.
Bioorganic & Medicinal Chemistry
|
May 22, 2003
Acyl sulfonamides as potent protease inhibitors of the hepatitis C virus full-Length NS3 (protease-helicase/NTPase): a comparative study of different C-terminals
Anja Johansson, Anton Poliakov, Eva Akerblom, et al.
Journal of Medicinal Chemistry
|
January 25, 2008
Two-carbon-elongated HIV-1 protease inhibitors with a tertiary-alcohol-containing transition-state mimic
Xiongyu Wu, Per Ohrngren, Jenny K Ekegren, et al.
Biochemistry
|
August 31, 2006
Inhibitor binding to the plasmepsin IV aspartic protease from Plasmodium falciparum
Hugo Gutiérrez-de-Terán, Martin Nervall, Karolina Ersmark, et al.
Bioorganic & Medicinal Chemistry
|
May 6, 2006
Potent inhibitors of the hepatitis C virus NS3 protease: use of a novel P2 cyclopentane-derived template
Per-Ola Johansson, Marcus Bäck, Ingemar Kvarnström, et al.
Bioorganic & Medicinal Chemistry
|
July 5, 2008
Selective angiotensin II AT2 receptor agonists: Benzamide structure-activity relationships
Charlotta Wallinder, Milad Botros, Ulrika Rosenström, et al.
European Journal of Medicinal Chemistry
|
December 29, 2009
Synthesis of potent BACE-1 inhibitors incorporating a hydroxyethylene isostere as central core
Fredrik Wångsell, Karin Gustafsson, Ingemar Kvarnström, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 109) with videos related to
Sort By:
Page
of 11
Journal of Medicinal Chemistry
|
March 3, 2006
Microwave-accelerated synthesis of P1'-extended HIV-1 protease inhibitors encompassing a tertiary alcohol in the transition-state mimicking scaffold
Jenny K Ekegren, Nina Ginman, Asa Johansson, et al.
Journal of Medicinal Chemistry
|
April 12, 2011
Potent macrocyclic inhibitors of insulin-regulated aminopeptidase (IRAP) by olefin ring-closing metathesis
Hanna Andersson, Heidi Demaegdt, Anders Johnsson, et al.
Plos One
|
April 23, 2014
Direct angiotensin AT2 receptor stimulation using a novel AT2 receptor agonist, compound 21, evokes neuroprotection in conscious hypertensive rats
Claudia A McCarthy, Antony Vinh, Alyson A Miller, et al.
Bioorganic & Medicinal Chemistry
|
November 17, 2006
Synthesis of novel potent hepatitis C virus NS3 protease inhibitors: discovery of 4-hydroxy-cyclopent-2-ene-1,2-dicarboxylic acid as a N-acyl-L-hydroxyproline bioisostere
Fredrik Thorstensson, Fredrik Wångsell, Ingemar Kvarnström, et al.
Bioorganic & Medicinal Chemistry
|
May 22, 2003
Acyl sulfonamides as potent protease inhibitors of the hepatitis C virus full-Length NS3 (protease-helicase/NTPase): a comparative study of different C-terminals
Anja Johansson, Anton Poliakov, Eva Akerblom, et al.
Journal of Medicinal Chemistry
|
January 25, 2008
Two-carbon-elongated HIV-1 protease inhibitors with a tertiary-alcohol-containing transition-state mimic
Xiongyu Wu, Per Ohrngren, Jenny K Ekegren, et al.
Biochemistry
|
August 31, 2006
Inhibitor binding to the plasmepsin IV aspartic protease from Plasmodium falciparum
Hugo Gutiérrez-de-Terán, Martin Nervall, Karolina Ersmark, et al.
Bioorganic & Medicinal Chemistry
|
May 6, 2006
Potent inhibitors of the hepatitis C virus NS3 protease: use of a novel P2 cyclopentane-derived template
Per-Ola Johansson, Marcus Bäck, Ingemar Kvarnström, et al.
Bioorganic & Medicinal Chemistry
|
July 5, 2008
Selective angiotensin II AT2 receptor agonists: Benzamide structure-activity relationships
Charlotta Wallinder, Milad Botros, Ulrika Rosenström, et al.
European Journal of Medicinal Chemistry
|
December 29, 2009
Synthesis of potent BACE-1 inhibitors incorporating a hydroxyethylene isostere as central core
Fredrik Wångsell, Karin Gustafsson, Ingemar Kvarnström, et al.
Page
of 11