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BindingDB contains 3.1M data for 1.3M Compounds and 9.6K Targets. Of those, 1.5M data for 708K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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37 articles for thisTarget


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

PMID
Data
Article Title
Organization
Potent, Selective, and Cell Active Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor Developed by Structure-Based Virtual Screening and Hit Optimization.EBI
Shandong University
Discovery of a Dual PRMT5-PRMT7 Inhibitor.EBI
University of Toronto
Development of Macrocyclic PRMT5-Adaptor Protein Interaction Inhibitors.EBI
Max Planck Institute of Molecular Physiology
Fragment-Based Discovery of MRTX1719, a Synthetic Lethal Inhibitor of the PRMT5•MTA Complex for the Treatment of EBI
Mirati Therapeutics
Discovery of a First-in-Class Inhibitor of the PRMT5-Substrate Adaptor Interaction.EBI
The Broad Institute of Mit and Harvard
A Chemical Probe for the Methyl Transferase PRMT5 with a Novel Binding Mode.EBI
Janssen Pharmaceutica
Discovery of First-in-Class Protein Arginine Methyltransferase 5 (PRMT5) Degraders.EBI
Icahn School of Medicine At Mount Sinai
Structure and Property Guided Design in the Identification of PRMT5 Tool Compound EPZ015666.EBI
Epizyme
Pharmacophore-based screening of diamidine small molecule inhibitors for protein arginine methyltransferases.EBI
University of Georgia
Allosteric Modulation of Protein Arginine Methyltransferase 5 (PRMT5).EBI
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.EBI
Shanghai Institute of Materia Medica
Nucleoside protein arginine methyltransferase 5 (PRMT5) inhibitors.EBI
Prelude Therapeutics
Discovery of new potent protein arginine methyltransferase 5 (PRMT5) inhibitors by assembly of key pharmacophores from known inhibitors.EBI
University of Jinan
Discovery of Potent and Selective Covalent Protein Arginine Methyltransferase 5 (PRMT5) Inhibitors.EBI
Prelude Therapeutics
Protein Arginine Methyltransferase 5 (PRMT5) as an Anticancer Target and Its Inhibitor Discovery.EBI
Sun Yat-Sen University
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity.EBI
Lilly Research Laboratories
Identification of a novel selective small-molecule inhibitor of protein arginine methyltransferase 5 (PRMT5) by virtual screening, resynthesis and biological evaluations.EBI
University of Jinan
PYRROLIDINE DERIVATIVES AS DDRS INHIBITORSBDB
Chiesi Farmaceutici
GPR35 Agonist CompoundsBDB
Heptares Therapeutics Limited
Peptide derivatives and uses thereofBDB
Nosopharm
Amino alcohol derivative, pharmaceutical composition and application thereofBDB
Beijing Foreland Pharma
Deuterated compounds as rock inhibitorsBDB
Fochon Pharmaceuticals
Prostate-specific membrane antigen targeted high-affinity agents for endoradiotherapy of prostate cancerBDB
The Johns Hopkins University
Pyrazolotriazolopyrimidine derivatives as A2A receptor antagonistBDB
Beigene
Compounds useful as RET inhibitorsBDB
Cancer Research Technology
Imidazotriaines and imidazopyrimidines as kinase inhibitorsBDB
Incyte Holdings
Compositions for treating neurodegenerative diseasesBDB
Cognition Therapeutics
Ectonucleotidase inhibitors and methods of use thereofBDB
Calithera Biosciences
Azaspiro[4.5]decane derivatives and use thereofBDB
Purdue Pharma
Substituted indoline derivatives as dengue viral replication inhibitorsBDB
Janssen Pharmaceuticals
4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulatorsBDB
Heptares Therapeutics
Azetidine derivativesBDB
Vernalis (R&D)
Development of Potent, Selective SRPK1 Inhibitors as Potential Topical Therapeutics for Neovascular Eye Disease.BDB
Exonate
Pyrazole compoundsBDB
Eli Lilly
Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetesBDB
Merck Sharpe & Dohme