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19 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Discovery and Characterization of a Highly Potent and Selective Aminopyrazoline-Based in Vivo Probe (BAY-598) for the Protein Lysine Methyltransferase SMYD2.EBI
Bayer Pharma
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2.EBI
Abbvie
Selective inhibitors of protein methyltransferases.EBI
Icahn School of Medicine At Mount Sinai
SAH derived potent and selective EZH2 inhibitors.EBI
Pfizer
Discovery of a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8.EBI
University of North Carolina At Chapel Hill
Oncoepigenomics: making histone lysine methylation count.EBI
TBA
Positioning of an unprecedented 1,5-oxaza spiroquinone scaffold into SMYD2 inhibitors in epigenetic space.EBI
Gachon University
Protein Lysine Methyltransferase SMYD2: A Promising Small Molecule Target for Cancer Therapy.EBI
Zhejiang University
HIV latency reversal agents: A potential path for functional cure?EBI
S£O Paulo State University (Unesp)
Synthesis and structure-activity relationship studies of LLY-507 analogues as SMYD2 inhibitors.EBI
Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University)
Design, Synthesis, and Biological Activity of Substrate Competitive SMYD2 Inhibitors.EBI
Astrazeneca
Histone methyl transferases: A class of epigenetic opportunities to counter uncontrolled cell proliferation.EBI
Punjabi University
Selective, Small-Molecule Co-Factor Binding Site Inhibition of a Su(var)3-9, Enhancer of Zeste, Trithorax Domain Containing Lysine Methyltransferase.EBI
Pfizer
Novel Oxindole Sulfonamides and Sulfamides: EPZ031686, the First Orally Bioavailable Small Molecule SMYD3 Inhibitor.EBI
Epizyme
Discovery of Bisubstrate Inhibitors of Nicotinamide N-Methyltransferase (NNMT).EBI
Icahn School of Medicine At Mount Sinai
Discovery of phenyl acetic acid substituted quinolines as novel liver X receptor agonists for the treatment of atherosclerosis.BDB
Wyeth Research
Protein farnesyltransferase inhibitors exhibit potent antimalarial activity.BDB
University of Washington At Seattle