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Showing results (11-20 of 23) with videos related to

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Journal of Molecular Biology|April 13, 2010
X-ray structures of the LXRalpha LBD in its homodimeric form and implications for heterodimer signalingXavier Fradera, Diep Vu, Olaf Nimz, et al.
Bioorganic & Medicinal Chemistry Letters|June 5, 2003
Novel water soluble 2,6-dimethoxyphenyl ester derivatives with intravenous anaesthetic activityD Jonathan Bennett, Alison Anderson, Kirsteen Buchanan, et al.
Journal of Medicinal Chemistry|April 19, 2002
Cyclodextrin-derived host molecules as reversal agents for the neuromuscular blocker rocuronium bromide: synthesis and structure-activity relationshipsJulia M Adam, D Jonathan Bennett, Anton Bom, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2010
4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically importantJiaqiang Cai, Xavier Fradera, Mario van Zeeland, et al.
Bioorganic & Medicinal Chemistry Letters|January 14, 2011
1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors: separation of desired cellular activity from undesired tissue accumulation through optimization of basic nitrogen pkaWullie Arbuckle, Mark Baugh, Simone Belshaw, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2016
Imidazopyridyl compounds as aldosterone synthase inhibitorsBrent R Whitehead, Michael M-C Lo, Amjad Ali, et al.
Bioorganic & Medicinal Chemistry Letters|October 30, 2010
Trifluoromethylphenyl as P2 for ketoamide-based cathepsin S inhibitorsJiaqiang Cai, John Robinson, Simone Belshaw, et al.
Bioorganic & Medicinal Chemistry Letters|July 3, 2010
2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitorsJiaqiang Cai, D Jonathan Bennett, Zoran Rankovic, et al.
Bioorganic & Medicinal Chemistry Letters|July 6, 2010
6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitorsJiaqiang Cai, Mark Baugh, Darcey Black, et al.
Journal of Medicinal Chemistry|March 25, 2016
Identification and in Vivo Evaluation of Liver X Receptor β-Selective Agonists for the Potential Treatment of Alzheimer's DiseaseShawn J Stachel, Celina Zerbinatti, Michael T Rudd, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of Molecular Biology|April 13, 2010
X-ray structures of the LXRalpha LBD in its homodimeric form and implications for heterodimer signalingXavier Fradera, Diep Vu, Olaf Nimz, et al.
Bioorganic & Medicinal Chemistry Letters|June 5, 2003
Novel water soluble 2,6-dimethoxyphenyl ester derivatives with intravenous anaesthetic activityD Jonathan Bennett, Alison Anderson, Kirsteen Buchanan, et al.
Journal of Medicinal Chemistry|April 19, 2002
Cyclodextrin-derived host molecules as reversal agents for the neuromuscular blocker rocuronium bromide: synthesis and structure-activity relationshipsJulia M Adam, D Jonathan Bennett, Anton Bom, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2010
4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically importantJiaqiang Cai, Xavier Fradera, Mario van Zeeland, et al.
Bioorganic & Medicinal Chemistry Letters|January 14, 2011
1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors: separation of desired cellular activity from undesired tissue accumulation through optimization of basic nitrogen pkaWullie Arbuckle, Mark Baugh, Simone Belshaw, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2016
Imidazopyridyl compounds as aldosterone synthase inhibitorsBrent R Whitehead, Michael M-C Lo, Amjad Ali, et al.
Bioorganic & Medicinal Chemistry Letters|October 30, 2010
Trifluoromethylphenyl as P2 for ketoamide-based cathepsin S inhibitorsJiaqiang Cai, John Robinson, Simone Belshaw, et al.
Bioorganic & Medicinal Chemistry Letters|July 3, 2010
2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitorsJiaqiang Cai, D Jonathan Bennett, Zoran Rankovic, et al.
Bioorganic & Medicinal Chemistry Letters|July 6, 2010
6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitorsJiaqiang Cai, Mark Baugh, Darcey Black, et al.
Journal of Medicinal Chemistry|March 25, 2016
Identification and in Vivo Evaluation of Liver X Receptor β-Selective Agonists for the Potential Treatment of Alzheimer's DiseaseShawn J Stachel, Celina Zerbinatti, Michael T Rudd, et al.
Pageof 3