The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 748K Compounds and 4.8K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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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
Treatment of conditions associated with hyperinsulinaemiaBDB
Tensha Therapeutics
Indazole compounds and uses thereofBDB
Incyte
Apoptosis signal-regulating kinase inhibitorsBDB
Gilead Sciences
Modulators of the prostacyclin (PGI2) receptor useful for the treatment of disorders related theretoBDB
Arena Pharmaceuticals
Imidazopyridines and imidazopyrazines as LSD1 inhibitorsBDB
Incyte
Deuterated diaminopyrimidine compounds and pharmaceutical compositions comprising such compoundsBDB
Suzhou Zelgen Biopharmaceuticals
Acetyl-CoA carboxylase modulatorsBDB
Monsanto Technology
Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disordersBDB
Galapagos
Discovery of a Novel Inhibitor of Coronavirus 3CL Protease as a Clinical Candidate for the Potential Treatment of COVID-19.BDB
Pfizer
Purinones as ubiquitin-specific protease 1 inhibitorsBDB
Forma Therapeutics
Substituted B-amino acid derivatives as CXCR3 receptor antagonistsBDB
Sanofi
Fluoroalkyl and fluorocycloalkyl 1,4-benzodiazepinone compoundsBDB
Bristol-Myers Squibb
Pyridine derivativesBDB
Hoffmann-La Roche
Substituted 4-aminocyclohexane derivativesBDB
Gruenenthal
Triazolo compounds as PDE10 inhibitorsBDB
Hoffmann-La Roche
Compound for increasing kinase active and application thereofBDB
Fujian Haixi Pharmaceuticals
Novel N-hydroxybenzamides incorporating 2-oxoindoline with unexpected potent histone deacetylase inhibitory effects and antitumor cytotoxicity.BDB
Hanoi University of Pharmacy
Synthesis and anti-acetylcholinesterase activity of scopoletin derivatives.BDB
Chulabhorn Research Institute
Structure and Inhibition of Microbiome ß-Glucuronidases Essential to the Alleviation of Cancer Drug Toxicity.BDB
University of North Carolina at Chapel Hill