37 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Potent, Selective, and Cell Active Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor Developed by Structure-Based Virtual Screening and Hit Optimization.

Shandong University
Discovery of a Dual PRMT5-PRMT7 Inhibitor.

University of Toronto
Development of Macrocyclic PRMT5-Adaptor Protein Interaction Inhibitors.

Max Planck Institute of Molecular Physiology
Fragment-Based Discovery of MRTX1719, a Synthetic Lethal Inhibitor of the PRMT5•MTA Complex for the Treatment of

Mirati Therapeutics
Discovery of a First-in-Class Inhibitor of the PRMT5-Substrate Adaptor Interaction.

The Broad Institute of Mit and Harvard
A Chemical Probe for the Methyl Transferase PRMT5 with a Novel Binding Mode.

Janssen Pharmaceutica
Discovery of First-in-Class Protein Arginine Methyltransferase 5 (PRMT5) Degraders.

Icahn School of Medicine At Mount Sinai
Structure and Property Guided Design in the Identification of PRMT5 Tool Compound EPZ015666.

Epizyme
Pharmacophore-based screening of diamidine small molecule inhibitors for protein arginine methyltransferases.

University of Georgia
Allosteric Modulation of Protein Arginine Methyltransferase 5 (PRMT5).

Merck
Discovery of 2-substituted-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide as potent and selective protein arginine methyltransferases 5 inhibitors: Design, synthesis and biological evaluation.

Shanghai Institute of Materia Medica
Nucleoside protein arginine methyltransferase 5 (PRMT5) inhibitors.

Prelude Therapeutics
Discovery of new potent protein arginine methyltransferase 5 (PRMT5) inhibitors by assembly of key pharmacophores from known inhibitors.

University of Jinan
Discovery of Potent and Selective Covalent Protein Arginine Methyltransferase 5 (PRMT5) Inhibitors.

Prelude Therapeutics
Protein Arginine Methyltransferase 5 (PRMT5) as an Anticancer Target and Its Inhibitor Discovery.

Sun Yat-Sen University
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity.

Lilly Research Laboratories
Identification of a novel selective small-molecule inhibitor of protein arginine methyltransferase 5 (PRMT5) by virtual screening, resynthesis and biological evaluations.

University of Jinan
PYRROLIDINE DERIVATIVES AS DDRS INHIBITORS

Chiesi Farmaceutici
GPR35 Agonist Compounds

Heptares Therapeutics Limited
Peptide derivatives and uses thereof

Nosopharm
Amino alcohol derivative, pharmaceutical composition and application thereof

Beijing Foreland Pharma
Deuterated compounds as rock inhibitors

Fochon Pharmaceuticals
Prostate-specific membrane antigen targeted high-affinity agents for endoradiotherapy of prostate cancer

The Johns Hopkins University
Pyrazolotriazolopyrimidine derivatives as A2A receptor antagonist

Beigene
Compounds useful as RET inhibitors

Cancer Research Technology
Imidazotriaines and imidazopyrimidines as kinase inhibitors

Incyte Holdings
Compositions for treating neurodegenerative diseases

Cognition Therapeutics
Ectonucleotidase inhibitors and methods of use thereof

Calithera Biosciences
Azaspiro[4.5]decane derivatives and use thereof

Purdue Pharma
Substituted indoline derivatives as dengue viral replication inhibitors

Janssen Pharmaceuticals
4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators

Heptares Therapeutics
Azetidine derivatives

Vernalis (R&D)
Development of Potent, Selective SRPK1 Inhibitors as Potential Topical Therapeutics for Neovascular Eye Disease.

Exonate
Pyrazole compounds

Eli Lilly
Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes

Merck Sharpe & Dohme