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Journal of Medicinal Chemistry|June 3, 2017
Design, Multicomponent Synthesis, and Anticancer Activity of a Focused Histone Deacetylase (HDAC) Inhibitor Library with Peptoid-Based Cap GroupsViktoria Krieger, Alexandra Hamacher, Christoph G W Gertzen, 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 schistosomiasisEhab 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 ActivityTino Heimburg, Fiona R Kolbinger, Patrik Zeyen, et al.
Journal of Medicinal Chemistry|January 16, 2019
Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 InhibitorsKatharina Vögerl, Nghia Ong, Johanna Senger, et al.
European Journal of Medicinal Chemistry|March 20, 2022
Identification of histone deacetylase 10 (HDAC10) inhibitors that modulate autophagy in transformed cellsPatrik Zeyen, Yanira Zeyn, Daniel Herp, et al.
Chemmedchem|October 17, 2022
Chemically Diverse S. mansoni HDAC8 Inhibitors Reduce Viability in Worm Larval and Adult StagesBeatrice Noce, Elisabetta Di Bello, Clemens Zwergel, et al.
Journal of Medicinal Chemistry|June 7, 2024
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD+-Dependent Lysine Deacylase Sirtuin 2Arianna Colcerasa, Florian Friedrich, Jelena Melesina, et al.
Cell Reports|September 6, 2024
The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domainsMarina Vitoria Gomes, Pauline Landwerlin, Marie-Laure Diebold-Durand, et al.
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