Synthesis and in vitro evaluation of diverse heterocyclic diphenolic compounds as inhibitors of DYRK1A.

Autor: Zhou Q; School of Chemistry, The University of Sydney, New South Wales 2006, Australia., Reekie TA; School of Chemistry, The University of Sydney, New South Wales 2006, Australia., Abbassi RH; School of Medical Sciences, Discipline of Pathology and Charles Perkins Centre, The University of Sydney, New South Wales 2006, Australia., Indurthi Venkata D; School of Medical Sciences, Discipline of Pathology and Charles Perkins Centre, The University of Sydney, New South Wales 2006, Australia., Font JS; School of Medical Sciences, Discipline of Pharmacology, The University of Sydney, New South Wales 2006, Australia., Ryan RM; School of Medical Sciences, Discipline of Pharmacology, The University of Sydney, New South Wales 2006, Australia., Munoz L; School of Medical Sciences, Discipline of Pathology and Charles Perkins Centre, The University of Sydney, New South Wales 2006, Australia., Kassiou M; School of Chemistry, The University of Sydney, New South Wales 2006, Australia. Electronic address: michael.kassiou@sydney.edu.au.
Jazyk: angličtina
Zdroj: Bioorganic & medicinal chemistry [Bioorg Med Chem] 2018 Dec 01; Vol. 26 (22), pp. 5852-5869. Date of Electronic Publication: 2018 Oct 28.
DOI: 10.1016/j.bmc.2018.10.034
Abstrakt: Dual-specificity tyrosine phosphorylation-related kinase 1A (DYRK1A) is a dual-specificity protein kinase that catalyses phosphorylation and autophosphorylation. Higher DYRK1A expression correlates with cancer, in particular glioblastoma present within the brain. We report here the synthesis and biological evaluation of new heterocyclic diphenolic derivatives designed as novel DYRK1A inhibitors. The generation of these heterocycles such as benzimidazole, imidazole, naphthyridine, pyrazole-pyridines, bipyridine, and triazolopyrazines was made based on the structural modification of the lead DANDY and tested for their ability to inhibit DYRK1A. None of these derivatives showed significant DYRK1A inhibition but provide valuable knowledge around the importance of the 7-azaindole moiety. These data will be of use for developing further structure-activity relationship studies to improve the selective inhibition of DYRK1A.
(Copyright © 2018 Elsevier Ltd. All rights reserved.)
Databáze: MEDLINE
Externí odkaz: