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Journal of Medicinal Chemistry
|
January 16, 2019
Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 Inhibitors
Katharina Vögerl, Nghia Ong, Johanna Senger, et al.
Journal of Medicinal Chemistry
|
January 22, 2024
Specific Inhibitors of Mitochondrial Deacylase Sirtuin 4 Endowed with Cellular Activity
Martin Pannek, Zayan Alhalabi, Daniela Tomaselli, et al.
European Journal of Medicinal Chemistry
|
August 15, 2021
Synthesis, structure-activity relationships, cocrystallization and cellular characterization of novel smHDAC8 inhibitors for the treatment of schistosomiasis
Ehab Ghazy, Tino Heimburg, Julien Lancelot, et al.
Journal of Medicinal Chemistry
|
December 1, 2017
Structure-Based Design and Biological Characterization of Selective Histone Deacetylase 8 (HDAC8) Inhibitors with Anti-Neuroblastoma Activity
Tino Heimburg, Fiona R Kolbinger, Patrik Zeyen, et al.
Journal of Medicinal Chemistry
|
November 30, 2022
Development of Alkylated Hydrazides as Highly Potent and Selective Class I Histone Deacetylase Inhibitors with T cell Modulatory Properties
Ping Sun, Jing Wang, Khadija S Khan, et al.
European Journal of Medicinal Chemistry
|
March 20, 2022
Identification of histone deacetylase 10 (HDAC10) inhibitors that modulate autophagy in transformed cells
Patrik Zeyen, Yanira Zeyn, Daniel Herp, et al.
Chemmedchem
|
October 17, 2022
Chemically Diverse S. mansoni HDAC8 Inhibitors Reduce Viability in Worm Larval and Adult Stages
Beatrice Noce, Elisabetta Di Bello, Clemens Zwergel, et al.
International Journal of Molecular Sciences
|
June 2, 2021
Structure-Based Design, Docking and Binding Free Energy Calculations of A366 Derivatives as Spindlin1 Inhibitors
Chiara Luise, Dina Robaa, Pierre Regenass, et al.
Journal of Medicinal Chemistry
|
June 7, 2024
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD<sup>+</sup>-Dependent Lysine Deacylase Sirtuin 2
Arianna Colcerasa, Florian Friedrich, Jelena Melesina, et al.
Journal of Medicinal Chemistry
|
October 23, 2018
Characterization of Histone Deacetylase 8 (HDAC8) Selective Inhibition Reveals Specific Active Site Structural and Functional Determinants
Martin Marek, Tajith B Shaik, Tino Heimburg, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Journal of Medicinal Chemistry
|
January 16, 2019
Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 Inhibitors
Katharina Vögerl, Nghia Ong, Johanna Senger, et al.
Journal of Medicinal Chemistry
|
January 22, 2024
Specific Inhibitors of Mitochondrial Deacylase Sirtuin 4 Endowed with Cellular Activity
Martin Pannek, Zayan Alhalabi, Daniela Tomaselli, et al.
European Journal of Medicinal Chemistry
|
August 15, 2021
Synthesis, structure-activity relationships, cocrystallization and cellular characterization of novel smHDAC8 inhibitors for the treatment of schistosomiasis
Ehab Ghazy, Tino Heimburg, Julien Lancelot, et al.
Journal of Medicinal Chemistry
|
December 1, 2017
Structure-Based Design and Biological Characterization of Selective Histone Deacetylase 8 (HDAC8) Inhibitors with Anti-Neuroblastoma Activity
Tino Heimburg, Fiona R Kolbinger, Patrik Zeyen, et al.
Journal of Medicinal Chemistry
|
November 30, 2022
Development of Alkylated Hydrazides as Highly Potent and Selective Class I Histone Deacetylase Inhibitors with T cell Modulatory Properties
Ping Sun, Jing Wang, Khadija S Khan, et al.
European Journal of Medicinal Chemistry
|
March 20, 2022
Identification of histone deacetylase 10 (HDAC10) inhibitors that modulate autophagy in transformed cells
Patrik Zeyen, Yanira Zeyn, Daniel Herp, et al.
Chemmedchem
|
October 17, 2022
Chemically Diverse S. mansoni HDAC8 Inhibitors Reduce Viability in Worm Larval and Adult Stages
Beatrice Noce, Elisabetta Di Bello, Clemens Zwergel, et al.
International Journal of Molecular Sciences
|
June 2, 2021
Structure-Based Design, Docking and Binding Free Energy Calculations of A366 Derivatives as Spindlin1 Inhibitors
Chiara Luise, Dina Robaa, Pierre Regenass, et al.
Journal of Medicinal Chemistry
|
June 7, 2024
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD<sup>+</sup>-Dependent Lysine Deacylase Sirtuin 2
Arianna Colcerasa, Florian Friedrich, Jelena Melesina, et al.
Journal of Medicinal Chemistry
|
October 23, 2018
Characterization of Histone Deacetylase 8 (HDAC8) Selective Inhibition Reveals Specific Active Site Structural and Functional Determinants
Martin Marek, Tajith B Shaik, Tino Heimburg, et al.
Page
of 8