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 698K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

If BindingDB was of value to your research, please take a moment to donate to this nonprofit project. Your donation will let us provide you with more data and improved service.

To help with training and testing AI and other models, BindingDB downloads and search results now provide the publication date and BindingDB curation date of each measurement.

30 articles for thisTarget


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

PMID
Data
Article Title
Organization
Orally active PDE4 inhibitors with therapeutic potential.EBI
Minase Research Institute
New orally active PDE4 inhibitors with therapeutic potential.EBI
Minase Research Institute
Highly potent PDE4 inhibitors with therapeutic potential.EBI
Minase Research Institute
Synthesis and evaluation of¿-lactam analogs of PGE2 as EP4 and EP2/EP4 agonists.EBI
Minase Research Institute
Discovery of orally available spirodiketopiperazine-based CCR5 antagonists.EBI
Minase Research Institute
Discovery of long-acting N-(cyanomethyl)-N-alkyl-L-prolinamide inhibitors of dipeptidyl peptidase IV.EBI
Minase Research Institute
Discovery of new chemical leads for prostaglandin D2 receptor antagonists.EBI
Minase Research Institute
Discovery of novel prostaglandin analogs as potent and selective EP2/EP4 dual agonists.EBI
Minase Research Institute
Pyrrolo[1,2-b]pyridazines, pyrrolo[2,1-f]triazin-4(3H)-ones, and related compounds as novel corticotropin-releasing factor 1 (CRF¿?) receptor antagonists.EBI
Minase Research Institute
Discovery of a novel EP2/EP4 dual agonist with high subtype-selectivity.EBI
Minase Research Institute
Synthesis and evaluation of novel modified¿-lactam prostanoids as EP4 subtype-selective agonists.EBI
Minase Research Institute
Pyrazolo[1,5-a]pyrimidines, triazolo[1,5-a]pyrimidines and their tricyclic derivatives as corticotropin-releasing factor 1 (CRF¿?) receptor antagonists.EBI
Minase Research Institute
Design and synthesis of new prostaglandin D2 receptor antagonists.EBI
Minase Research Institute
6,7-Dihydro-5H-cyclopenta[d]pyrazolo[1,5-a]pyrimidines and their derivatives as novel corticotropin-releasing factor 1 receptor antagonists.EBI
Minase Research Institute
Discovery of selective indole-based prostaglandin D2 receptor antagonist.EBI
Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. Part 3: Synthesis, metabolic stability, and biological evaluation of optically active analogs.EBI
Minase Research Institute
Discovery of novel N-acylsulfonamide analogs as potent and selective EP3 receptor antagonists.EBI
Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. Part 1: discovery and exploration of the carboxyamide side chain.EBI
Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. part 2: optimization of the side chains to improve in vitro and in vivo potencies.EBI
Minase Research Institute
Spirodiketopiperazine-based CCR5 antagonists: Improvement of their pharmacokinetic profiles.EBI
Minase Research Institute
Design and synthesis of new potent dipeptidyl peptidase IV inhibitors with enhanced ex vivo duration.EBI
Minase Research Institute
Design and synthesis of long-acting inhibitors of dipeptidyl peptidase IV.EBI
Minase Research Institute
Discovery of orally active prostaglandin D2 receptor antagonists.EBI
Minase Research Institute
Clarification of mechanism of human sputum elastase inhibition by a new inhibitor, ONO-5046, using electrospray ionization mass spectrometry.EBI
Minase Research Institute
L-Cysteine based N-type calcium channel blockers: structure-activity relationships of the C-terminal lipophilic moiety, and oral analgesic efficacy in rat pain models.EBI
Minase Research Institute
Structure-activity study of L-cysteine-based N-type calcium channel blockers: optimization of N- and C-terminal substituents.EBI
Minase Research Institute
Design and synthesis of a highly selective EP4-receptor agonist. Part 2: 5-thia and 9beta-haloPG derivatives with improved stability.EBI
Minase Research Institute
Design and synthesis of a highly selective EP4-receptor agonist. Part 1: 3,7-dithiaPG derivatives with high selectivity.EBI
Minase Research Institute
Design and synthesis of a highly selective EP2-receptor agonist.EBI
Minase Research Institute
New orally active serine protease inhibitors.EBI
Minase Research Institute