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Joseph J McDonald

Showing results (1-10 of 15) with videos related to

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Journal of Chemical Theory and Computation|March 25, 2016
Molecular Dynamics Analysis of Binding of Kinase Inhibitors to WT EGFR and the T790M MutantJiyong Park, Joseph J McDonald, Russell C Petter, et al.
ACS Medicinal Chemistry Letters|December 21, 2019
Evolution of Cereblon-Mediated Protein Degradation as a Therapeutic ModalityPhilip P Chamberlain, Laura A D'Agostino, J Michael Ellis, et al.
Journal of Medicinal Chemistry|February 10, 2011
Discovery of potent inhibitors of soluble epoxide hydrolase by combinatorial library design and structure-based virtual screeningLi Xing, Joseph J McDonald, Steve A Kolodziej, et al.
Journal of Chemical Information and Computer Sciences|May 25, 2004
Assessment of docking poses: interactions-based accuracy classification (IBAC) versus crystal structure deviationsRomano T Kroemer, Anna Vulpetti, Joseph J McDonald, et al.
Bioorganic & Medicinal Chemistry Letters|June 10, 2010
MMP-13 selective isonipecotamide alpha-sulfone hydroxamatesStephen A Kolodziej, Susan L Hockerman, Gary A DeCrescenzo, et al.
Biochimica Et Biophysica Acta|July 31, 2002
Solution structure and backbone dynamics of the catalytic domain of matrix metalloproteinase-2 complexed with a hydroxamic acid inhibitorYiqing Feng, John J Likos, Leiming Zhu, et al.
Journal of Computer-Aided Molecular Design|September 9, 2008
Homo-timeric structural model of human microsomal prostaglandin E synthase-1 and characterization of its substrate/inhibitor binding interactionsLi Xing, Ravi G Kurumbail, Ronald B Frazier, et al.
Bioorganic & Medicinal Chemistry Letters|June 10, 2010
Orally bioavailable dual MMP-1/MMP-14 sparing, MMP-13 selective alpha-sulfone hydroxamatesStephen A Kolodziej, Susan L Hockerman, Terri L Boehm, et al.
Bioorganic & Medicinal Chemistry|October 15, 2003
Discovery of novel benzothiazolesulfonamides as potent inhibitors of HIV-1 proteaseSrinivasan R Nagarajan, Gary A De Crescenzo, Daniel P Getman, et al.
Bioorganic & Medicinal Chemistry Letters|October 20, 2006
Design of potent inhibitors of human beta-secretase. Part 2John N Freskos, Yvette M Fobian, Timothy E Benson, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Chemical Theory and Computation|March 25, 2016
Molecular Dynamics Analysis of Binding of Kinase Inhibitors to WT EGFR and the T790M MutantJiyong Park, Joseph J McDonald, Russell C Petter, et al.
ACS Medicinal Chemistry Letters|December 21, 2019
Evolution of Cereblon-Mediated Protein Degradation as a Therapeutic ModalityPhilip P Chamberlain, Laura A D'Agostino, J Michael Ellis, et al.
Journal of Medicinal Chemistry|February 10, 2011
Discovery of potent inhibitors of soluble epoxide hydrolase by combinatorial library design and structure-based virtual screeningLi Xing, Joseph J McDonald, Steve A Kolodziej, et al.
Journal of Chemical Information and Computer Sciences|May 25, 2004
Assessment of docking poses: interactions-based accuracy classification (IBAC) versus crystal structure deviationsRomano T Kroemer, Anna Vulpetti, Joseph J McDonald, et al.
Bioorganic & Medicinal Chemistry Letters|June 10, 2010
MMP-13 selective isonipecotamide alpha-sulfone hydroxamatesStephen A Kolodziej, Susan L Hockerman, Gary A DeCrescenzo, et al.
Biochimica Et Biophysica Acta|July 31, 2002
Solution structure and backbone dynamics of the catalytic domain of matrix metalloproteinase-2 complexed with a hydroxamic acid inhibitorYiqing Feng, John J Likos, Leiming Zhu, et al.
Journal of Computer-Aided Molecular Design|September 9, 2008
Homo-timeric structural model of human microsomal prostaglandin E synthase-1 and characterization of its substrate/inhibitor binding interactionsLi Xing, Ravi G Kurumbail, Ronald B Frazier, et al.
Bioorganic & Medicinal Chemistry Letters|June 10, 2010
Orally bioavailable dual MMP-1/MMP-14 sparing, MMP-13 selective alpha-sulfone hydroxamatesStephen A Kolodziej, Susan L Hockerman, Terri L Boehm, et al.
Bioorganic & Medicinal Chemistry|October 15, 2003
Discovery of novel benzothiazolesulfonamides as potent inhibitors of HIV-1 proteaseSrinivasan R Nagarajan, Gary A De Crescenzo, Daniel P Getman, et al.
Bioorganic & Medicinal Chemistry Letters|October 20, 2006
Design of potent inhibitors of human beta-secretase. Part 2John N Freskos, Yvette M Fobian, Timothy E Benson, et al.
Pageof 2