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Journal of Medicinal Chemistry
|
January 25, 2014
De-novo designed library of benzoylureas as inhibitors of BCL-XL: synthesis, structural and biochemical characterization
Ryan M Brady, Amelia Vom, Michael J Roy, et al.
Journal of Biomolecular Screening
|
November 17, 2011
An efficient high-throughput screening method for MYST family acetyltransferases, a new class of epigenetic drug targets
Hendrik Falk, Theresa Connor, Hong Yang, et al.
Journal of Proteome Research
|
May 23, 2013
Characterization of the novel broad-spectrum kinase inhibitor CTx-0294885 as an affinity reagent for mass spectrometry-based kinome profiling
Luxi Zhang, Ian P Holmes, Falko Hochgräfe, et al.
Journal of Medicinal Chemistry
|
March 4, 2011
Quinazoline sulfonamides as dual binders of the proteins B-cell lymphoma 2 and B-cell lymphoma extra long with potent proapoptotic cell-based activity
Brad E Sleebs, Peter E Czabotar, Wayne J Fairbrother, et al.
Cell Reports
|
October 21, 2020
Temporal Analysis of Brd4 Displacement in the Control of B Cell Survival, Proliferation, and Differentiation
Isabella Y Kong, Joel S Rimes, Amanda Light, et al.
Nature Chemical Biology
|
April 23, 2013
Structure-guided design of a selective BCL-X(L) inhibitor
Guillaume Lessene, Peter E Czabotar, Brad E Sleebs, et al.
Journal of Medicinal Chemistry
|
June 18, 2013
Discovery of potent and selective benzothiazole hydrazone inhibitors of Bcl-XL
Brad E Sleebs, Wilhemus J A Kersten, Sanji Kulasegaram, et al.
Journal of Medicinal Chemistry
|
July 2, 2019
Discovery of Benzoylsulfonohydrazides as Potent Inhibitors of the Histone Acetyltransferase KAT6A
David J Leaver, Benjamin Cleary, Nghi Nguyen, et al.
Biorxiv : the Preprint Server for Biology
|
December 23, 2024
Catalytic inhibition of KAT6/KAT7 enhances the efficacy and overcomes primary and acquired resistance to Menin inhibitors in MLL leukaemia
Shellaina J V Gordon, Florian Perner, Laura MacPherson, et al.
Journal of Medicinal Chemistry
|
March 3, 2020
Discovery of Acylsulfonohydrazide-Derived Inhibitors of the Lysine Acetyltransferase, KAT6A, as Potent Senescence-Inducing Anti-Cancer Agents
Daniel L Priebbenow, David J Leaver, Nghi Nguyen, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Journal of Medicinal Chemistry
|
January 25, 2014
De-novo designed library of benzoylureas as inhibitors of BCL-XL: synthesis, structural and biochemical characterization
Ryan M Brady, Amelia Vom, Michael J Roy, et al.
Journal of Biomolecular Screening
|
November 17, 2011
An efficient high-throughput screening method for MYST family acetyltransferases, a new class of epigenetic drug targets
Hendrik Falk, Theresa Connor, Hong Yang, et al.
Journal of Proteome Research
|
May 23, 2013
Characterization of the novel broad-spectrum kinase inhibitor CTx-0294885 as an affinity reagent for mass spectrometry-based kinome profiling
Luxi Zhang, Ian P Holmes, Falko Hochgräfe, et al.
Journal of Medicinal Chemistry
|
March 4, 2011
Quinazoline sulfonamides as dual binders of the proteins B-cell lymphoma 2 and B-cell lymphoma extra long with potent proapoptotic cell-based activity
Brad E Sleebs, Peter E Czabotar, Wayne J Fairbrother, et al.
Cell Reports
|
October 21, 2020
Temporal Analysis of Brd4 Displacement in the Control of B Cell Survival, Proliferation, and Differentiation
Isabella Y Kong, Joel S Rimes, Amanda Light, et al.
Nature Chemical Biology
|
April 23, 2013
Structure-guided design of a selective BCL-X(L) inhibitor
Guillaume Lessene, Peter E Czabotar, Brad E Sleebs, et al.
Journal of Medicinal Chemistry
|
June 18, 2013
Discovery of potent and selective benzothiazole hydrazone inhibitors of Bcl-XL
Brad E Sleebs, Wilhemus J A Kersten, Sanji Kulasegaram, et al.
Journal of Medicinal Chemistry
|
July 2, 2019
Discovery of Benzoylsulfonohydrazides as Potent Inhibitors of the Histone Acetyltransferase KAT6A
David J Leaver, Benjamin Cleary, Nghi Nguyen, et al.
Biorxiv : the Preprint Server for Biology
|
December 23, 2024
Catalytic inhibition of KAT6/KAT7 enhances the efficacy and overcomes primary and acquired resistance to Menin inhibitors in MLL leukaemia
Shellaina J V Gordon, Florian Perner, Laura MacPherson, et al.
Journal of Medicinal Chemistry
|
March 3, 2020
Discovery of Acylsulfonohydrazide-Derived Inhibitors of the Lysine Acetyltransferase, KAT6A, as Potent Senescence-Inducing Anti-Cancer Agents
Daniel L Priebbenow, David J Leaver, Nghi Nguyen, et al.
Page
of 6