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Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors | Journal of Medicinal Chemistry
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Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors | Journal of Medicinal Chemistry
Discovery of a Selective, Substrate-Competitive Inhibitor of the Lysine Methyltransferase SETD8 | Journal of Medicinal Chemistry
Clinical studies with oral/IV glutamine (Gln) supplementation in head... | Download Table
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Targeting Enhancer of Zeste Homolog 2 for the Treatment of Hematological Malignancies and Solid Tumors: Candidate Structure–Activity Relationships Insights and Evolution Prospects | Journal of Medicinal Chemistry
The m6A Writer: Rise of a Machine for Growing Tasks | Biochemistry
Covalent Small Molecule Immunomodulators Targeting the Protease Active Site | Journal of Medicinal Chemistry
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Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors | Journal of Medicinal Chemistry
PDF) M6A-Atlas: A comprehensive knowledgebase for unraveling the N6-methyladenosine (m6A) epitranscriptome
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