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The Journal of Organic Chemistry
|
August 26, 2006
Asymmetric synthesis of alpha,alpha-dibranched propargylamines by acetylide additions to N-tert-butanesulfinyl ketimines
Andrew W Patterson, Jonathan A Ellman
The Journal of Organic Chemistry
|
May 16, 2008
Expedient synthesis of N-methyl tubulysin analogues with high cytotoxicity
Andrew W Patterson, Hillary M Peltier, Jonathan A Ellman
Nature Protocols
|
April 5, 2007
Substrate activity screening (SAS): a general procedure for the preparation and screening of a fragment-based non-peptidic protease substrate library for inhibitor discovery
Andrew W Patterson, Warren J L Wood, Jonathan A Ellman
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
September 11, 2007
Design, synthesis, and biological properties of highly potent tubulysin D analogues
Andrew W Patterson, Hillary M Peltier, Florenz Sasse, et al.
Journal of the American Chemical Society
|
December 15, 2006
The total synthesis of tubulysin D
Hillary M Peltier, Jeffrey P McMahon, Andrew W Patterson, et al.
Journal of the American Chemical Society
|
November 3, 2005
Substrate activity screening: a fragment-based method for the rapid identification of nonpeptidic protease inhibitors
Warren J L Wood, Andrew W Patterson, Hiroyuki Tsuruoka, et al.
Journal of Medicinal Chemistry
|
October 13, 2006
Identification of selective, nonpeptidic nitrile inhibitors of cathepsin s using the substrate activity screening method
Andrew W Patterson, Warren J L Wood, Michael Hornsby, et al.
Chemical Science
|
February 17, 2015
Non-Directed Allylic C-H Acetoxylation in the Presence of Lewis Basic Heterocycles
Hasnain A Malik, Buck L H Taylor, John R Kerrigan, et al.
Bioorganic & Medicinal Chemistry
|
June 7, 2020
Discovery of a novel indole pharmacophore for the irreversible inhibition of myeloperoxidase (MPO)
Anup Patnaik, Laura Axford, Lin Deng, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 5, 2018
Discovery of 1-((6-Aminopyridin-3-yl)Methyl)-3-(4-Bromophenyl)Urea as a Potent, Irreversible Myeloperoxidase Inhibitor
Martin L Marro, Andrew W Patterson, Lac Lee, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
The Journal of Organic Chemistry
|
August 26, 2006
Asymmetric synthesis of alpha,alpha-dibranched propargylamines by acetylide additions to N-tert-butanesulfinyl ketimines
Andrew W Patterson, Jonathan A Ellman
The Journal of Organic Chemistry
|
May 16, 2008
Expedient synthesis of N-methyl tubulysin analogues with high cytotoxicity
Andrew W Patterson, Hillary M Peltier, Jonathan A Ellman
Nature Protocols
|
April 5, 2007
Substrate activity screening (SAS): a general procedure for the preparation and screening of a fragment-based non-peptidic protease substrate library for inhibitor discovery
Andrew W Patterson, Warren J L Wood, Jonathan A Ellman
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
September 11, 2007
Design, synthesis, and biological properties of highly potent tubulysin D analogues
Andrew W Patterson, Hillary M Peltier, Florenz Sasse, et al.
Journal of the American Chemical Society
|
December 15, 2006
The total synthesis of tubulysin D
Hillary M Peltier, Jeffrey P McMahon, Andrew W Patterson, et al.
Journal of the American Chemical Society
|
November 3, 2005
Substrate activity screening: a fragment-based method for the rapid identification of nonpeptidic protease inhibitors
Warren J L Wood, Andrew W Patterson, Hiroyuki Tsuruoka, et al.
Journal of Medicinal Chemistry
|
October 13, 2006
Identification of selective, nonpeptidic nitrile inhibitors of cathepsin s using the substrate activity screening method
Andrew W Patterson, Warren J L Wood, Michael Hornsby, et al.
Chemical Science
|
February 17, 2015
Non-Directed Allylic C-H Acetoxylation in the Presence of Lewis Basic Heterocycles
Hasnain A Malik, Buck L H Taylor, John R Kerrigan, et al.
Bioorganic & Medicinal Chemistry
|
June 7, 2020
Discovery of a novel indole pharmacophore for the irreversible inhibition of myeloperoxidase (MPO)
Anup Patnaik, Laura Axford, Lin Deng, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 5, 2018
Discovery of 1-((6-Aminopyridin-3-yl)Methyl)-3-(4-Bromophenyl)Urea as a Potent, Irreversible Myeloperoxidase Inhibitor
Martin L Marro, Andrew W Patterson, Lac Lee, et al.
Page
of 2