Novel Scaffolds for Dual Specificity Tyrosine-Phosphorylation-Regulated Kinase (DYRK1A) Inhibitors
Permanent lenke
https://hdl.handle.net/10037/14980Dato
2018-08-10Type
Journal articleTidsskriftartikkel
Peer reviewed
Forfatter
Czarna, Anna Lucja; Jinhua, Wang; Zelencova, Diana; Liu, Yao; Deng, Xianming; Choi, Hwan Geun; Zhang, Tinghu; Zhou, Wenjun; Chang, Jae Won; Kildalsen, Hanne; Seternes, Ole Morten; Gray, Nathanael S.; Engh, Richard Alan; Rothweiler, UlliSammendrag
DYRK1A is one of five members of the dual-specificity tyrosine (Y) phosphorylation-regulated kinase (DYRK)
family. The DYRK1A gene is located in the Down syndrome critical region and regulates cellular processes related to
proliferation and differentiation of neuronal progenitor cells during early development. This has focused research on its role in
neuronal degenerative diseases, including Alzheimer’s and Down syndrome. Recent studies have also shown a possible role of
DYRK1A in diabetes. Here we report a variety of scaffolds not generally known for DYRK1A inhibition, demonstrating their
effects in in vitro assays and also in cell cultures. These inhibitors effectively block the tau phosphorylation that is a hallmark of
Alzheimer’s disease. The crystal structures of these inhibitors support the design of optimized and novel therapeutics.
Beskrivelse
Accepted manuscript version. Published version available at https://doi.org/10.1021/acs.jmedchem.7b01847.