A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells

Cited by (807)

Items 801–807 of 807

  1. BindingDB Entry 50049189: Discovery of First-in-Class, Potent, and Orally Bioavailable Embryonic Ectoderm Development (EED) Inhibitor with Robust Anticancer Efficacy.
    BindingDB · 2019 · UC San Diego
  2. BindingDB Entry 50047123: The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat.
    BindingDB · 2017 · UC San Diego
  3. BindingDB Entry 50042555: Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitors.
    BindingDB · 2013 · UC San Diego
  4. BindingDB Entry 50015988: Histone Deacetylase and Enhancer of Zeste Homologue 2 Dual Inhibitors Presenting a Synergistic Effect for the Treatment of Hematological Malignancies.
    BindingDB · 2023 · UC San Diego
  5. BindingDB Entry 50010226: Structure-Activity Relationship Studies for Enhancer of Zeste Homologue 2 (EZH2) and Enhancer of Zeste Homologue 1 (EZH1) Inhibitors.
    BindingDB · 2021 · UC San Diego
  6. BindingDB Entry 50001605: Discovery of EBI-2511: A Highly Potent and Orally Active EZH2 Inhibitor for the Treatment of Non-Hodgkin's Lymphoma.
    BindingDB · 2020 · UC San Diego
  7. BindingDB Entry 7924: An allosteric PRC2 inhibitor targeting the H3K27me3 binding pocket of EED.
    BindingDB · 2017 · UC San Diego