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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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13 articles for SR Selness


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

PMID
Data
Article Title
Organization
Discovery of PH-797804, a highly selective and potent inhibitor of p38 MAP kinase.EBI
Pfizer
Discovery of N-substituted pyridinones as potent and selective inhibitors of p38 kinase.EBI
Pfizer
Design, synthesis and activity of a potent, selective series of N-aryl pyridinone inhibitors of p38 kinase.EBI
Pfizer
Substituted N-aryl-6-pyrimidinones: a new class of potent, selective, and orally active p38 MAP kinase inhibitors.EBI
Pfizer
Aminopyridinecarboxamide-based inhaled IKK-2 inhibitors for asthma and COPD: Structure-activity relationship.EBI
Pfizer
Discovery of 5-substituted-N-arylpyridazinones as inhibitors of p38 MAP kinase.EBI
Pfizer
Identification of SD-0006, a potent diaryl pyrazole inhibitor of p38 MAP kinase.EBI
Pfizer
Continued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition.EBI
Pfizer
Aminopyrazole Carboxamide Bruton's Tyrosine Kinase Inhibitors. Irreversible to Reversible Covalent Reactive Group Tuning.EBI
Pfizer
CONDENSED PYRAZOLE DERIVATIVES AS INHIBITORS OF SARM1BDB
Disarm Therapeutics
Nitrogen-containing polyhydroxylated aromatics as HIV-1 integrase inhibitors: synthesis, structure-activity relationship analysis, and biological activity.BDB
Shandong University
Picolinamido-propanoic acid derivatives useful as glucagon receptor antagonistsBDB
Janssen Pharmaceutica
Decreased binding affinity of olanzapine and clozapine for human muscarinic receptors in intact clonal cells in physiological medium.BDB
Eli Lilly