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John P Caldwell

Showing results (1-10 of 22) with videos related to

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Current Infectious Disease Reports|July 1, 2018
Evolving Epidemiology of Japanese Encephalitis: Implications for VaccinationJohn P Caldwell, Lin H Chen, Davidson H Hamer
Bioorganic & Medicinal Chemistry Letters|February 10, 2007
Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligandsJohn P Caldwell, Julius J Matasi, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2009
Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands: part 2John P Caldwell, Julius J Matasi, Xiomara Fernandez, et al.
Bioorganic & Medicinal Chemistry Letters|June 28, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: highly potent, orally active, adenosine A2A antagonists. Part 1Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2005
The discovery and synthesis of novel adenosine receptor (A(2A)) antagonistsJulius J Matasi, John P Caldwell, Jinsong Hao, et al.
Chemical Science|May 22, 2018
Protecting group free radical C-H trifluoromethylation of peptidesNaoko Ichiishi, John P Caldwell, Melissa Lin, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: the successful reduction of hERG activity. Part 2Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 20, 2007
3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonistsLisa S Silverman, John P Caldwell, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|July 21, 2016
Discovery of potent wall teichoic acid early stage inhibitorsMarc A Labroli, John P Caldwell, Christine Yang, et al.
Journal of Medicinal Chemistry|August 14, 2020
Generation of Leads for γ-Secretase ModulationMihirbaran Mandal, Alexei Buevich, John P Caldwell, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Current Infectious Disease Reports|July 1, 2018
Evolving Epidemiology of Japanese Encephalitis: Implications for VaccinationJohn P Caldwell, Lin H Chen, Davidson H Hamer
Bioorganic & Medicinal Chemistry Letters|February 10, 2007
Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligandsJohn P Caldwell, Julius J Matasi, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2009
Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands: part 2John P Caldwell, Julius J Matasi, Xiomara Fernandez, et al.
Bioorganic & Medicinal Chemistry Letters|June 28, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: highly potent, orally active, adenosine A2A antagonists. Part 1Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2005
The discovery and synthesis of novel adenosine receptor (A(2A)) antagonistsJulius J Matasi, John P Caldwell, Jinsong Hao, et al.
Chemical Science|May 22, 2018
Protecting group free radical C-H trifluoromethylation of peptidesNaoko Ichiishi, John P Caldwell, Melissa Lin, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: the successful reduction of hERG activity. Part 2Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 20, 2007
3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonistsLisa S Silverman, John P Caldwell, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|July 21, 2016
Discovery of potent wall teichoic acid early stage inhibitorsMarc A Labroli, John P Caldwell, Christine Yang, et al.
Journal of Medicinal Chemistry|August 14, 2020
Generation of Leads for γ-Secretase ModulationMihirbaran Mandal, Alexei Buevich, John P Caldwell, et al.
Pageof 3