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Journal of Medicinal Chemistry
|
May 13, 2015
New Monocyclic, Bicyclic, and Tricyclic Ethynylcyanodienones as Activators of the Keap1/Nrf2/ARE Pathway and Inhibitors of Inducible Nitric Oxide Synthase
Wei Li, Suqing Zheng, Maureen Higgins, et al.
Redox Biology
|
September 1, 2020
Isomeric O-methyl cannabidiolquinones with dual BACH1/NRF2 activity
Laura Casares, Juan Diego Unciti-Broceta, Maria Eugenia Prados, et al.
Bioorganic & Medicinal Chemistry
|
February 7, 2012
Synthesis and biological characterisation of sirtuin inhibitors based on the tenovins
Anna R McCarthy, Lisa Pirrie, Jonathan J Hollick, et al.
Iscience
|
January 17, 2022
The isoquinoline PRL-295 increases the thermostability of Keap1 and disrupts its interaction with Nrf2
Sharadha Dayalan Naidu, Takafumi Suzuki, Dina Dikovskaya, et al.
Journal of Medicinal Chemistry
|
May 13, 2022
Phenyl Bis-Sulfonamide Keap1-Nrf2 Protein-Protein Interaction Inhibitors with an Alternative Binding Mode
Nikolaos Georgakopoulos, Sandeep Talapatra, Dina Dikovskaya, et al.
Molecular Cancer Therapeutics
|
January 17, 2013
Tenovin-D3, a novel small-molecule inhibitor of sirtuin SirT2, increases p21 (CDKN1A) expression in a p53-independent manner
Anna R McCarthy, Marijke C C Sachweh, Maureen Higgins, et al.
Iscience
|
October 26, 2020
Downregulation of Keap1 Confers Features of a Fasted Metabolic State
Elena V Knatko, Michael H Tatham, Ying Zhang, et al.
Redox Biology
|
November 16, 2025
Tetrazole-containing naphthalene bis-sulfonamide Keap1-Nrf2 interaction inhibitors with unexpected binding modes
Nikolaos D Georgakopoulos, Sandeep K Talapatra, Sharadha Dayalan Naidu, et al.
Redox Biology
|
July 27, 2025
Identification of a BACH1 lung cancer signature: A novel tool for understanding BACH1 biology and identifying new inhibitors
Donika Klenja-Skudrinja, Kevin X Ali, David Walker, et al.
Cell Cycle (Georgetown, Tex.)
|
October 31, 2008
Characterization, chemical optimization and anti-tumour activity of a tubulin poison identified by a p53-based phenotypic screen
Oliver D Staples, Jonathan J Hollick, Johanna Campbell, et al.
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Search research articles
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Showing results (31-40 of 53) with videos related to
Sort By:
Page
of 6
Journal of Medicinal Chemistry
|
May 13, 2015
New Monocyclic, Bicyclic, and Tricyclic Ethynylcyanodienones as Activators of the Keap1/Nrf2/ARE Pathway and Inhibitors of Inducible Nitric Oxide Synthase
Wei Li, Suqing Zheng, Maureen Higgins, et al.
Redox Biology
|
September 1, 2020
Isomeric O-methyl cannabidiolquinones with dual BACH1/NRF2 activity
Laura Casares, Juan Diego Unciti-Broceta, Maria Eugenia Prados, et al.
Bioorganic & Medicinal Chemistry
|
February 7, 2012
Synthesis and biological characterisation of sirtuin inhibitors based on the tenovins
Anna R McCarthy, Lisa Pirrie, Jonathan J Hollick, et al.
Iscience
|
January 17, 2022
The isoquinoline PRL-295 increases the thermostability of Keap1 and disrupts its interaction with Nrf2
Sharadha Dayalan Naidu, Takafumi Suzuki, Dina Dikovskaya, et al.
Journal of Medicinal Chemistry
|
May 13, 2022
Phenyl Bis-Sulfonamide Keap1-Nrf2 Protein-Protein Interaction Inhibitors with an Alternative Binding Mode
Nikolaos Georgakopoulos, Sandeep Talapatra, Dina Dikovskaya, et al.
Molecular Cancer Therapeutics
|
January 17, 2013
Tenovin-D3, a novel small-molecule inhibitor of sirtuin SirT2, increases p21 (CDKN1A) expression in a p53-independent manner
Anna R McCarthy, Marijke C C Sachweh, Maureen Higgins, et al.
Iscience
|
October 26, 2020
Downregulation of Keap1 Confers Features of a Fasted Metabolic State
Elena V Knatko, Michael H Tatham, Ying Zhang, et al.
Redox Biology
|
November 16, 2025
Tetrazole-containing naphthalene bis-sulfonamide Keap1-Nrf2 interaction inhibitors with unexpected binding modes
Nikolaos D Georgakopoulos, Sandeep K Talapatra, Sharadha Dayalan Naidu, et al.
Redox Biology
|
July 27, 2025
Identification of a BACH1 lung cancer signature: A novel tool for understanding BACH1 biology and identifying new inhibitors
Donika Klenja-Skudrinja, Kevin X Ali, David Walker, et al.
Cell Cycle (Georgetown, Tex.)
|
October 31, 2008
Characterization, chemical optimization and anti-tumour activity of a tubulin poison identified by a p53-based phenotypic screen
Oliver D Staples, Jonathan J Hollick, Johanna Campbell, et al.
Page
of 6