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Frontiers | The Roles of Histone Deacetylases and Their Inhibitors in Cancer Therapy
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Chemically Induced Degradation of Sirtuin 2 (Sirt2) by a Proteolysis Targeting Chimera (PROTAC) Based on Sirtuin Rearranging Ligands (SirReals) | Journal of Medicinal Chemistry
Structure–Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2) | Journal of Medicinal Chemistry
Chemically Induced Degradation of Sirtuin 2 (Sirt2) by a Proteolysis Targeting Chimera (PROTAC) Based on Sirtuin Rearranging Ligands (SirReals) | Journal of Medicinal Chemistry
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Identification of Diketopiperazine-Containing 2-Anilinobenzamides as Potent Sirtuin 2 (SIRT2)-Selective Inhibitors Targeting the “Selectivity Pocket”, Substrate-Binding Site, and NAD+-Binding Site | Journal of Medicinal Chemistry
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Structure–Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2) | Journal of Medicinal Chemistry
Frontiers | The Roles of Histone Deacetylases and Their Inhibitors in Cancer Therapy
Frontiers | The Roles of Histone Deacetylases and Their Inhibitors in Cancer Therapy
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Structure–Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2) | Journal of Medicinal Chemistry