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15 articles for thisTarget


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

PMID
Data
Article Title
Organization
Chemical and biological investigation of N-hydroxy-valdecoxib: An active metabolite of valdecoxib.EBI
Gedeon Richter
HR1405-01, a Safe intravenous NSAID with superior anti-inflammatory and analgesic activities in preclinical trials.EBI
China Pharmaceutical University
Imidazolylacetophenone oxime-based multifunctional neuroprotective agents: Discovery and structure-activity relationships.EBI
Northwest A&F University
-2-(Phenylamino) Benzamide Derivatives as Dual Inhibitors of COX-2 and Topo I Deter Gastrointestinal Cancers via Targeting Inflammation and Tumor Progression.EBI
Lanzhou University
Resveratrol-based compounds and neurodegeneration: Recent insight in multitarget therapy.EBI
"G. D'Annunzio" University of Chieti-Pescara
Discovery of dual inhibitors of topoisomerase I and Cyclooxygenase-2 for colon cancer therapy.EBI
Lanzhou University
Pyridazine as a privileged structure: An updated review on anticancer activity of pyridazine containing bioactive molecules.EBI
Key Laboratory of Technology of Drug Preparation (Zhengzhou University)
Contemporary advances of cyclic molecules proposed for inflammation.EBI
Dpsr University
From the Design to the EBI
Unitat Associada Al Csic
Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents.EBI
University of Malakand
Fragment-Based Discovery of Novel Allosteric MEK1 Binders.EBI
Astrazeneca
Transformation of Santonin to a Naproxen Analogue with Anti-Inflammatory Activity.EBI
Indian Institute of Integrative Medicine (Csir)
Cyclic enaminone as new chemotype for selective cyclooxygenase-2 inhibitory, anti-inflammatory, and analgesic activities.EBI
National Institute of Pharmaceutical Education and Research (NIPER)
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid.EBI
University of Torino
Hydroxytriazole derivatives as potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors discovered by bioisosteric scaffold hopping approach.EBI
University of Torino