15 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Recent advances in nuclear receptor-binding SET domain 2 (NSD2) inhibitors: An update and perspectives.

China Pharmaceutical University
NSD3: Advances in cancer therapeutic potential and inhibitors research.

Peking University
Drug Discovery Targeting Nuclear Receptor Binding SET Domain Protein 2 (NSD2).

University of Texas Medical Branch (UTMB)
Discovery of a New-Generation S-Adenosylmethionine-Noncompetitive Covalent Inhibitor Targeting the Lysine Methyltransferase Enhancer of Zeste Homologue 2.

Sun Yat-Sen University
Structural Modification and Pharmacological Evaluation of Substituted Quinoline-5,8-diones as Potent NSD2 Inhibitors.

Shanghai Jiao Tong University
Structure-Aided Design, Synthesis, and Biological Evaluation of Potent and Selective Non-Nucleoside Inhibitors Targeting Protein Arginine Methyltransferase 5.

Sun Yat-Sen University
Discovery of a First-in-Class Degrader for Nuclear Receptor Binding SET Domain Protein 2 (NSD2) and Ikaros/Aiolos.

Icahn School of Medicine At Mount Sinai
Structure-Based Discovery of a Series of NSD2-PWWP1 Inhibitors.

Chinese Academy of Sciences
5-Aminonaphthalene derivatives as selective nonnucleoside nuclear receptor binding SET domain-protein 2 (NSD2) inhibitors for the treatment of multiple myeloma.

Chinese Academy of Sciences
Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2.

University of Toronto
Computational discovery and biological evaluation of novel inhibitors targeting histone-lysine N-methyltransferase SET7.

China Pharmaceutical University
Novel inhibitors of As(III) S-adenosylmethionine methyltransferase (AS3MT) identified by virtual screening.

Astrazeneca
Spirotricycle RIPK1 inhibitors and methods of uses thereof

Merck Sharp & Dohme
Sulfonamide-substituted cyanopyrrolidines with activity as DUB inhibitors

Mission Therapeutics
Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes

Merck Sharpe & Dohme