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Yipin Lu

Showing results (31-40 of 39) with videos related to

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Journal of Medicinal Chemistry|October 1, 2004
Structure-based discovery of nonpeptidic small organic compounds to block the T cell response to myelin basic proteinNiklas K U Koehler, Chao-Yie Yang, Judith Varady, et al.
Journal of Medicinal Chemistry|November 3, 2010
4-(Pyrazol-4-yl)-pyrimidines as selective inhibitors of cyclin-dependent kinase 4/6Young Shin Cho, Maria Borland, Christopher Brain, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2008
Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibitionSanjeev Shangary, Dongguang Qin, Donna McEachern, et al.
Journal of Medicinal Chemistry|March 20, 2018
Discovery and Optimization of Phosphopantetheine Adenylyltransferase Inhibitors with Gram-Negative Antibacterial ActivityColin K Skepper, Robert J Moreau, Brent A Appleton, et al.
Chembiochem : a European Journal of Chemical Biology|April 18, 2023
Discovery of Potent Pyrazoline-Based Covalent SARS-CoV-2 Main Protease InhibitorsPatrick Moon, Charlotte M Zammit, Qian Shao, et al.
Journal of the American Chemical Society|December 9, 2022
An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4Angel Gonzalez-Valero, Audrey G Reeves, Annika C S Page, et al.
Journal of Medicinal Chemistry|May 27, 2017
Design, Synthesis, and Properties of a Potent Inhibitor of Pseudomonas aeruginosa Deacetylase LpxCGrazia Piizzi, David T Parker, Yunshan Peng, et al.
Journal of Medicinal Chemistry|March 3, 2018
Fragment-Based Drug Discovery of Inhibitors of Phosphopantetheine Adenylyltransferase from Gram-Negative BacteriaRobert J Moreau, Colin K Skepper, Brent A Appleton, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Fragment-Based Discovery of 7-Azabenzimidazoles as Potent, Highly Selective, and Orally Active CDK4/6 InhibitorsYoung Shin Cho, Hayley Angove, Christopher Brain, et al.
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Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Medicinal Chemistry|October 1, 2004
Structure-based discovery of nonpeptidic small organic compounds to block the T cell response to myelin basic proteinNiklas K U Koehler, Chao-Yie Yang, Judith Varady, et al.
Journal of Medicinal Chemistry|November 3, 2010
4-(Pyrazol-4-yl)-pyrimidines as selective inhibitors of cyclin-dependent kinase 4/6Young Shin Cho, Maria Borland, Christopher Brain, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2008
Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibitionSanjeev Shangary, Dongguang Qin, Donna McEachern, et al.
Journal of Medicinal Chemistry|March 20, 2018
Discovery and Optimization of Phosphopantetheine Adenylyltransferase Inhibitors with Gram-Negative Antibacterial ActivityColin K Skepper, Robert J Moreau, Brent A Appleton, et al.
Chembiochem : a European Journal of Chemical Biology|April 18, 2023
Discovery of Potent Pyrazoline-Based Covalent SARS-CoV-2 Main Protease InhibitorsPatrick Moon, Charlotte M Zammit, Qian Shao, et al.
Journal of the American Chemical Society|December 9, 2022
An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4Angel Gonzalez-Valero, Audrey G Reeves, Annika C S Page, et al.
Journal of Medicinal Chemistry|May 27, 2017
Design, Synthesis, and Properties of a Potent Inhibitor of Pseudomonas aeruginosa Deacetylase LpxCGrazia Piizzi, David T Parker, Yunshan Peng, et al.
Journal of Medicinal Chemistry|March 3, 2018
Fragment-Based Drug Discovery of Inhibitors of Phosphopantetheine Adenylyltransferase from Gram-Negative BacteriaRobert J Moreau, Colin K Skepper, Brent A Appleton, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Fragment-Based Discovery of 7-Azabenzimidazoles as Potent, Highly Selective, and Orally Active CDK4/6 InhibitorsYoung Shin Cho, Hayley Angove, Christopher Brain, et al.
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