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Journal of Medicinal Chemistry|April 10, 2019
Selective Inhibition of Histone Deacetylase 10: Hydrogen Bonding to the Gatekeeper Residue is ImplicatedMagalie Géraldy, Michael Morgen, Peter Sehr, et al.Cell Reports|May 25, 2024
Decrypting lysine deacetylase inhibitor action and protein modifications by dose-resolved proteomicsYun-Chien Chang, Christian Gnann, Raphael R Steimbach, et al.Nature Chemistry|February 20, 2025
Site-specific activation of the proton pump inhibitor rabeprazole by tetrathiolate zinc centresTeresa Marker, Raphael R Steimbach, Cecilia Perez-Borrajero, et al.Chemmedchem|April 30, 2020
Design and Synthesis of Dihydroxamic Acids as HDAC6/8/10 InhibitorsMichael Morgen, Raphael R Steimbach, Magalie Géraldy, et al.Chembiochem : a European Journal of Chemical Biology|May 24, 2022
First Fluorescent Acetylspermidine Deacetylation Assay for HDAC10 Identifies Selective Inhibitors with Cellular Target EngagementDaniel Herp, Johannes Ridinger, Dina Robaa, et al.Journal of the American Chemical Society|October 6, 2022
Aza-SAHA Derivatives Are Selective Histone Deacetylase 10 Chemical Probes That Inhibit Polyamine Deacetylation and Phenocopy HDAC10 KnockoutRaphael R Steimbach, Corey J Herbst-Gervasoni, Severin Lechner, et al.Nature Chemical Biology|April 28, 2022
Target deconvolution of HDAC pharmacopoeia reveals MBLAC2 as common off-targetSeverin Lechner, Martin Ian P Malgapo, Christian Grätz, et al.Pageof 2