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James P Edwards

Showing results (11-20 of 71) with videos related to

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Bioorganic & Medicinal Chemistry Letters|May 11, 2010
Agonist/antagonist modulation in a series of 2-aryl benzimidazole H4 receptor ligandsBrad M Savall, James P Edwards, Jennifer D Venable, et al.
Organic Letters|September 26, 2018
Minisci-Photoredox-Mediated α-Heteroarylation of N-Protected Secondary Amines: Remarkable Selectivity of AzetidinesCyril Bosset, Hélène Beucher, Guillaume Bretel, et al.
Bioorganic & Medicinal Chemistry Letters|April 25, 2008
Dual binding site inhibitors of B-RAF kinaseRonald L Wolin, Scott D Bembenek, Jianmei Wei, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2015
Diaminopyrimidines, diaminopyridines and diaminopyridazines as histamine H4 receptor modulatorsBrad M Savall, Steven P Meduna, Kevin Tays, et al.
Bioorganic & Medicinal Chemistry Letters|January 15, 2013
Pyrazole-based arylalkyne cathepsin S inhibitors. Part III: modification of P4 regionJohn J M Wiener, Alvah Tyson Wickboldt, Steven Nguyen, et al.
Journal of Medicinal Chemistry|September 17, 2004
Nonpeptidic, noncovalent inhibitors of the cysteine protease cathepsin SRobin L Thurmond, Mary Pat Beavers, Hui Cai, et al.
Bioorganic & Medicinal Chemistry Letters|December 3, 2014
The effect of pK(a) on pyrimidine/pyridine-derived histamine H4 ligandsBrad M Savall, Steven P Meduna, Jennifer Venable, et al.
Bioorganic & Medicinal Chemistry Letters|September 8, 2007
Pyrazole-based cathepsin S inhibitors with improved cellular potencyJianmei Wei, Barbara A Pio, Hui Cai, et al.
Bioorganic & Medicinal Chemistry Letters|June 5, 2003
Synthesis and biological activity of 5-methylidene 1,2-dihydrochromeno[3,4-f]quinoline derivatives as progesterone receptor modulatorsLin Zhi, Christopher M Tegley, Barbara Pio, et al.
Journal of Medicinal Chemistry|February 6, 2014
Discovery and SAR of 6-alkyl-2,4-diaminopyrimidines as histamine H₄ receptor antagonistsBrad M Savall, Frank Chavez, Kevin Tays, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Bioorganic & Medicinal Chemistry Letters|May 11, 2010
Agonist/antagonist modulation in a series of 2-aryl benzimidazole H4 receptor ligandsBrad M Savall, James P Edwards, Jennifer D Venable, et al.
Organic Letters|September 26, 2018
Minisci-Photoredox-Mediated α-Heteroarylation of N-Protected Secondary Amines: Remarkable Selectivity of AzetidinesCyril Bosset, Hélène Beucher, Guillaume Bretel, et al.
Bioorganic & Medicinal Chemistry Letters|April 25, 2008
Dual binding site inhibitors of B-RAF kinaseRonald L Wolin, Scott D Bembenek, Jianmei Wei, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2015
Diaminopyrimidines, diaminopyridines and diaminopyridazines as histamine H4 receptor modulatorsBrad M Savall, Steven P Meduna, Kevin Tays, et al.
Bioorganic & Medicinal Chemistry Letters|January 15, 2013
Pyrazole-based arylalkyne cathepsin S inhibitors. Part III: modification of P4 regionJohn J M Wiener, Alvah Tyson Wickboldt, Steven Nguyen, et al.
Journal of Medicinal Chemistry|September 17, 2004
Nonpeptidic, noncovalent inhibitors of the cysteine protease cathepsin SRobin L Thurmond, Mary Pat Beavers, Hui Cai, et al.
Bioorganic & Medicinal Chemistry Letters|December 3, 2014
The effect of pK(a) on pyrimidine/pyridine-derived histamine H4 ligandsBrad M Savall, Steven P Meduna, Jennifer Venable, et al.
Bioorganic & Medicinal Chemistry Letters|September 8, 2007
Pyrazole-based cathepsin S inhibitors with improved cellular potencyJianmei Wei, Barbara A Pio, Hui Cai, et al.
Bioorganic & Medicinal Chemistry Letters|June 5, 2003
Synthesis and biological activity of 5-methylidene 1,2-dihydrochromeno[3,4-f]quinoline derivatives as progesterone receptor modulatorsLin Zhi, Christopher M Tegley, Barbara Pio, et al.
Journal of Medicinal Chemistry|February 6, 2014
Discovery and SAR of 6-alkyl-2,4-diaminopyrimidines as histamine H₄ receptor antagonistsBrad M Savall, Frank Chavez, Kevin Tays, et al.
Pageof 8