Literature DB >> 28766366

Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) inhibitors: a survey of recent patent literature.

Thu Lan Nguyen1,2,3,4,5, Corinne Fruit6, Yann Hérault1,2,3,4,5, Laurent Meijer1, Thierry Besson6.   

Abstract

INTRODUCTION: Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a eukaryotic serine-threonine protein kinase belonging to the CMGC group. DYRK1A hyperactivity appears to contribute to the development of a number of human malignancies and to cognitive deficits observed in Down syndrome and Alzheimer's disease. As a result, the DYRK1A kinase represents an attractive target for the synthesis and optimization of pharmacological inhibitors of potential therapeutic interest. Like most tyrosine kinase inhibitors developed up to the market, DYRK1A inhibitors are essentially acting by competing with ATP for binding at the catalytic site of the kinase. Areas covered: This paper reviews patent activity associated with the discovery of synthetic novel heterocyclic molecules inhibiting the catalytic activity of DYRK1A. Expert opinion: Despite the important role of DYRK1A in biological processes and the growing interest in the design of new therapeutic drugs, there are only few patented synthetic DYRK1A inhibitors and most of them were and are still developed by academic research groups, sometimes with industrial partners.

Entities:  

Keywords:  Alzheimer’s disease; DYRK kinases; DYRK1A; down syndrome; heterocyclic compounds; kinase inhibitor; microwave chemistry; patents

Mesh:

Substances:

Year:  2017        PMID: 28766366     DOI: 10.1080/13543776.2017.1360285

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  18 in total

1.  Sexually dimorphic DYRK1A overexpression on postnatal day 15 in the Ts65Dn mouse model of Down syndrome: Effects of pharmacological targeting on behavioral phenotypes.

Authors:  Laura E Hawley; Faith Prochaska; Megan Stringer; Charles R Goodlett; Randall J Roper
Journal:  Pharmacol Biochem Behav       Date:  2022-05-14       Impact factor: 3.697

Review 2.  Marine-Derived 2-Aminoimidazolone Alkaloids. Leucettamine B-Related Polyandrocarpamines Inhibit Mammalian and Protozoan DYRK & CLK Kinases.

Authors:  Nadège Loaëc; Eletta Attanasio; Benoît Villiers; Emilie Durieu; Tania Tahtouh; Morgane Cam; Rohan A Davis; Aline Alencar; Mélanie Roué; Marie-Lise Bourguet-Kondracki; Peter Proksch; Emmanuelle Limanton; Solène Guiheneuf; François Carreaux; Jean-Pierre Bazureau; Michelle Klautau; Laurent Meijer
Journal:  Mar Drugs       Date:  2017-10-17       Impact factor: 5.118

3.  Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A.

Authors:  Thu Lan Nguyen; Arnaud Duchon; Antigoni Manousopoulou; Nadège Loaëc; Benoît Villiers; Guillaume Pani; Meltem Karatas; Anna E Mechling; Laura-Adela Harsan; Emmanuelle Limanton; Jean-Pierre Bazureau; François Carreaux; Spiros D Garbis; Laurent Meijer; Yann Herault
Journal:  Dis Model Mech       Date:  2018-09-27       Impact factor: 5.758

4.  Development of Kinase Inhibitors via Metal-Catalyzed C⁻H Arylation of 8-Alkyl-thiazolo[5,4-f]-quinazolin-9-ones Designed by Fragment-Growing Studies.

Authors:  Florence Couly; Marine Harari; Carole Dubouilh-Benard; Laetitia Bailly; Emilie Petit; Julien Diharce; Pascal Bonnet; Laurent Meijer; Corinne Fruit; Thierry Besson
Journal:  Molecules       Date:  2018-08-29       Impact factor: 4.411

5.  Indole-3-Carbonitriles as DYRK1A Inhibitors by Fragment-Based Drug Design.

Authors:  Rosanna Meine; Walter Becker; Hannes Falke; Lutz Preu; Nadège Loaëc; Laurent Meijer; Conrad Kunick
Journal:  Molecules       Date:  2018-01-24       Impact factor: 4.411

6.  Inhibition of DYRK1A proteolysis modifies its kinase specificity and rescues Alzheimer phenotype in APP/PS1 mice.

Authors:  Benoît Souchet; Mickael Audrain; Jean Marie Billard; Julien Dairou; Romain Fol; Nicola Salvatore Orefice; Satoru Tada; Yuchen Gu; Gaelle Dufayet-Chaffaud; Emmanuelle Limanton; François Carreaux; Jean-Pierre Bazureau; Sandro Alves; Laurent Meijer; Nathalie Janel; Jérôme Braudeau; Nathalie Cartier
Journal:  Acta Neuropathol Commun       Date:  2019-03-18       Impact factor: 7.801

7.  The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo.

Authors:  L Trovò; C Fuchs; R De Rosa; I Barbiero; M Tramarin; E Ciani; L Rusconi; C Kilstrup-Nielsen
Journal:  Neurobiol Dis       Date:  2020-02-04       Impact factor: 5.996

8.  [b]-Annulated Halogen-Substituted Indoles as Potential DYRK1A Inhibitors.

Authors:  Christian Lechner; Maren Flaßhoff; Hannes Falke; Lutz Preu; Nadége Loaëc; Laurent Meijer; Stefan Knapp; Apirat Chaikuad; Conrad Kunick
Journal:  Molecules       Date:  2019-11-13       Impact factor: 4.411

9.  Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype.

Authors:  Anne Walter; Apirat Chaikuad; Renate Helmer; Nadège Loaëc; Lutz Preu; Ingo Ott; Stefan Knapp; Laurent Meijer; Conrad Kunick
Journal:  PLoS One       Date:  2018-05-03       Impact factor: 3.240

Review 10.  DYRK1A Protein, A Promising Therapeutic Target to Improve Cognitive Deficits in Down Syndrome.

Authors:  Anis Feki; Youssef Hibaoui
Journal:  Brain Sci       Date:  2018-10-16
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