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Journal of the American Chemical Society
|
July 10, 2003
Asymmetric synthesis of (2S,3R)-capreomycidine and the total synthesis of capreomycin IB
Duane E DeMong, Robert M Williams
Organic Letters
|
May 30, 2013
A novel method for the preparation of 4-arylimidazolones
Duane E DeMong, Irene Ng, Michael W Miller, et al.
Journal of Medicinal Chemistry
|
October 13, 2007
Synthesis, structure-activity relationship and in vivo antiinflammatory efficacy of substituted dipiperidines as CCR2 antagonists
Mingde Xia, Cuifen Hou, Duane E DeMong, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 27, 2015
MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition
Matthew J Fell, Christian Mirescu, Kallol Basu, et al.
Journal of Medicinal Chemistry
|
May 5, 2026
Discovery of MK-1088 as a Potent A<sub>2A</sub>/A<sub>2B</sub> Adenosine Receptor Dual-Antagonist for Cancer Immunotherapy
Yonglian Zhang, Elisabeth Hennessy, Matthew A Larsen, et al.
Journal of Medicinal Chemistry
|
March 1, 2017
Discovery of a 3-(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity
Jack D Scott, Duane E DeMong, Thomas J Greshock, et al.
Journal of Medicinal Chemistry
|
December 8, 2022
Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1<i>H</i>-Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson's Disease
David A Candito, Vladimir Simov, Anmol Gulati, et al.
Journal of Medicinal Chemistry
|
April 29, 2026
Discovery of Potent and Selective Benzothiophene Difluoromethyl Phosphonate (DFMP) PTPN2/N1-Dual Inhibitors
Xiao Mei Zheng, David A Candito, James Jewell, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Journal of the American Chemical Society
|
July 10, 2003
Asymmetric synthesis of (2S,3R)-capreomycidine and the total synthesis of capreomycin IB
Duane E DeMong, Robert M Williams
Organic Letters
|
May 30, 2013
A novel method for the preparation of 4-arylimidazolones
Duane E DeMong, Irene Ng, Michael W Miller, et al.
Journal of Medicinal Chemistry
|
October 13, 2007
Synthesis, structure-activity relationship and in vivo antiinflammatory efficacy of substituted dipiperidines as CCR2 antagonists
Mingde Xia, Cuifen Hou, Duane E DeMong, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 27, 2015
MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition
Matthew J Fell, Christian Mirescu, Kallol Basu, et al.
Journal of Medicinal Chemistry
|
May 5, 2026
Discovery of MK-1088 as a Potent A<sub>2A</sub>/A<sub>2B</sub> Adenosine Receptor Dual-Antagonist for Cancer Immunotherapy
Yonglian Zhang, Elisabeth Hennessy, Matthew A Larsen, et al.
Journal of Medicinal Chemistry
|
March 1, 2017
Discovery of a 3-(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity
Jack D Scott, Duane E DeMong, Thomas J Greshock, et al.
Journal of Medicinal Chemistry
|
December 8, 2022
Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1<i>H</i>-Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson's Disease
David A Candito, Vladimir Simov, Anmol Gulati, et al.
Journal of Medicinal Chemistry
|
April 29, 2026
Discovery of Potent and Selective Benzothiophene Difluoromethyl Phosphonate (DFMP) PTPN2/N1-Dual Inhibitors
Xiao Mei Zheng, David A Candito, James Jewell, et al.
Page
of 1