The discovery of 2-amino-3,5-diarylbenzamide inhibitors of IKK-alpha and IKK-beta kinases

التفاصيل البيبلوغرافية
العنوان: The discovery of 2-amino-3,5-diarylbenzamide inhibitors of IKK-alpha and IKK-beta kinases
المؤلفون: Barbara G. Avitabile, Paul Bamborough, John A. Christopher, Michael J. Wilson, Aurelie C. Champigny, Geoffrey W. Mellor, Ken Grace, Jeremy D. A. Kitson, Nicholas Probst, Clive A. Smith, Champa Patel, Susan L. Dyos, William L. Rumsey, Jeffrey K. Kerns, James V. Morey, Mary A. Morse, Carolyn F. O’Malley, Geoffrey J. Cutler
المصدر: Bioorganicmedicinal chemistry letters. 17(14)
سنة النشر: 2007
مصطلحات موضوعية: Models, Molecular, Molecular model, cells, Clinical Biochemistry, Pharmaceutical Science, IκB kinase, environment and public health, Biochemistry, Drug Discovery, Enzyme Inhibitors, skin and connective tissue diseases, Molecular Biology, chemistry.chemical_classification, biology, Kinase, Organic Chemistry, Hydrogen Bonding, In vitro, Enzyme assay, I-kappa B Kinase, enzymes and coenzymes (carbohydrates), Enzyme, chemistry, Enzyme inhibitor, Benzamides, biology.protein, Molecular Medicine, biological phenomena, cell phenomena, and immunity, Signal transduction
الوصف: A potent and selective series of 2-amino-3,5-diarylbenzamide inhibitors of IKK-α and IKK-β is described. The most potent compounds are 8h , 8r and 8v , with IKK-β inhibitory potencies of pIC 50 7.0, 6.8 and 6.8, respectively. The series has excellent selectivity, both within the IKK family over IKK-e, and across a wide variety of kinase assays. The potency of 8h in the IKK-β enzyme assay translates to significant cellular activity (pIC 50 5.7–6.1) in assays of functional and mechanistic relevance.
تدمد: 0960-894X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::662d566d583ef34be934dd8aef6c31b8
https://pubmed.ncbi.nlm.nih.gov/17502144
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....662d566d583ef34be934dd8aef6c31b8
قاعدة البيانات: OpenAIRE