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

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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20 articles for thisTarget


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

PMID
Data
Article Title
Organization
Inhibitors of NEK7 kinaseBDB
Halia Therapeutics
3,4,5-trisubstituted-1,2,4-triazoles and 3,4,5-trisubstituted-3-thio-1,2,4-triazoles and uses thereofBDB
Board of Trustees of The Southern Illinois University
TYK2 inhibitors, uses, and methods for production thereofBDB
Nimbus Lakshmi
PDE9 inhibitor and use thereofBDB
Nanjing Transthera Biosciences
ErbB receptor inhibitorsBDB
TBA
Broad-spectrum non-covalent coronavirus protease inhibitorsBDB
Purdue Research Foundation
Piperazine derivatives for treating disordersBDB
The University of Nottingham
The role of a novel auxiliary pocket in bacterial phenylalanyl-tRNA synthetase druggability.BDB
Astrazeneca R&D Boston
Methods of modulating the activity of the MC5 receptor and treatment of conditions related to this receptorBDB
Mimetica
Acetamide derivatives as glucokinase activators, their process and medicinal applicationsBDB
Advinus Therapeutics
Synthesis, methods of using, and compositions of cycloalkylmethylaminesBDB
Reviva Pharmaceuticals
Aurora kinase inhibitors and methods of making and using thereofBDB
H. Lee Moffitt Cancer Center and Research Institute
Monoacylglycerol lipase inhibitors for the treatment of metabolic diseases and related disordersBDB
Janssen Pharmaceutica
Heteroaryl substituted indole compounds useful as MMP-13 inhibitorsBDB
Boehringer Ingelheim International
Synthesis, in vitro Biological Evaluation and Molecular Docking Studies of Benzimidamides as Potential BACE1 Inhibitors.BDB
Peking University Health Science Center
Identification and characterization of a second melanin-concentrating hormone receptor, MCH-2R.BDB
Merck Research Laboratories
Comparison of CGS 15943, ZM 241385 and SCH 58261 as antagonists at human adenosine receptors.BDB
Schering-Plough Research Institute
Pharmacological profiles for rat cortical M1 and M2 muscarinic receptors using selective antagonists: comparison with N1E-115 muscarinic receptors.BDB
Mayo Clinic