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BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 745K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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14 articles for PA Centrella


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

PMID
Data
Article Title
Organization
Discovery, SAR, and X-ray Binding Mode Study of BCATm Inhibitors from a Novel DNA-Encoded Library.EBI
Glaxosmithkline
Discovery of a Potent Class of PI3Ka Inhibitors with Unique Binding Mode via Encoded Library Technology (ELT).EBI
Glaxosmithkline
Metabolites of PPI-2458, a selective, irreversible inhibitor of methionine aminopeptidase-2: structure determination and in vivo activity.EBI
Glaxosmithkline
Encoded library technology as a source of hits for the discovery and lead optimization of a potent and selective class of bactericidal direct inhibitors of Mycobacterium tuberculosis InhA.EBI
Glaxosmithkline
Discovery of highly potent and selective small molecule ADAMTS-5 inhibitors that inhibit human cartilage degradation via encoded library technology (ELT).EBI
Glaxosmithkline
Identification and Evaluation of Reversible Covalent Binders to Cys55 of Bfl-1 from a DNA-Encoded Chemical Library Screen.EBI
AstraZeneca
Development of Potent Mcl-1 Inhibitors: Structural Investigations on Macrocycles Originating from a DNA-Encoded Chemical Library Screen.EBI
Symeres
Discovery of a First-in-Class Small-Molecule Ligand for WDR91 Using DNA-Encoded Chemical Library Selection Followed by Machine Learning.EBI
University of Toronto
Structure Based Design of Non-Natural Peptidic Macrocyclic Mcl-1 Inhibitors.EBI
Astrazeneca
Discovery of Novel UDP-EBI
X-Biotix Therapeutics
Novel irreversible covalent BTK inhibitors discovered using DNA-encoded chemistry.EBI
X-Chem
Discovery of soluble epoxide hydrolase inhibitors through DNA-encoded library technology (ELT).EBI
Gsk
Design, synthesis and biological evaluation of pazopanib derivatives as antitumor agents.BDB
Shandong Institute of Pharmaceutical Industry
Design of selective phenylglycine amide tissue factor/factor VIIa inhibitors.BDB
F. Hoffmann-La Roche