950763-07-2Relevant articles and documents
Design and Synthesis of Dihydroxamic Acids as HDAC6/8/10 Inhibitors
Christianson, David W.,Géraldy, Magalie,Gunkel, Nikolas,Hellweg, Lars,Herbst-Gervasoni, Corey J.,Miller, Aubry K.,Morgen, Michael,Oehme, Ina,Osko, Jeremy D.,Porter, Nicholas J.,Ridinger, Johannes,Sehr, Peter,Steimbach, Raphael R.,Witt, Olaf
, (2020/05/16)
We report the synthesis and evaluation of a class of selective multitarget agents for the inhibition of HDAC6, HDAC8, and HDAC10. The concept for this study grew out of a structural analysis of the two selective inhibitors Tubastatin A (HDAC6/10) and PCI-
INDOLE DERIVATIVES AS INHIBITORS OF HISTONE DEACETYLASE
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, (2008/06/13)
Described herein are compounds and pharmaceutical compositions containing such compounds, which inhibit the acitivy of histone deacetylase 8 (HDAC8). Also described herein are methods of using such HDAC8 inhibitors, alone and in combination with other compounds, for treating diseases or conditions that would benefit from inhibition of HDAC8 activity.