Efficient Two-Step Synthesis of Novel Pyrimido[4,5-d] Pyrimidines with Potent Neuroprotective, Antioxidant, and Aβ Anti-Aggregation Properties

Author:

Ben Ameur Ghada1,Maalej Emna2,Martin Helene3ORCID,Jacquinot Anne-Sophie3,Barbanneau Nadine4,Bernard Paul J.4,Marco-Contelles José56,Chabchoub Fakher1ORCID,Ismaili Lhassane4ORCID

Affiliation:

1. Laboratory of Applied Chemistry, Heterocycles, Lipids and Polymers, Faculty of Sciences of Sfax, University of Sfax, B.P. 802, Sfax 3000, Tunisia

2. Laboratoire Matériaux, Traitement et Analyse (LMTA), Institut National de Recherche et d’Analyse Physico-Chimique (INRAP), Ariana 2020, Tunisia

3. Université de Franche-Comté, EFS, INSERM, UMR RIGHT, F-25000 Besançon, France

4. Université de Franche-Comté, UMR INSERM 1322 LINC, F-25000 Besançon, France

5. Laboratory of Medicinal Chemistry (IQOG, CSIC), C/Juan de la Cierva 3, 28006 Madrid, Spain

6. Center for Biomedical Network Research on Rare Diseases (CIBERER), CIBER, ISCIII, 28006 Madrid, Spain

Abstract

Eleven new differently substituted N,7-diphenylpyrimido [4,5-d]pyrimidin-4-amines 4a–k were synthesized from readily available reagents in a simple and inexpensive two-step procedure with yields up to 57%. Neuroprotective analysis against H2O2 and analysis using ORAC assays identified compounds 4g, 4i and 4j as promising antioxidant compounds. These compounds also showed potent inhibition of Aβ1–42 self-aggregation, and suitable physicochemical properties predicted by Datawarior software V6.1.0, this biological activity and physicochemical property being of great interest for pathologies linked to oxidative stress, such as Alzheimer’s disease.

Funder

Regional Council of Franche-Comté

the French Ministry of Europe and Foreign Affairs

the Tunisian Ministry of Higher Education and Scientific Research

Publisher

MDPI AG

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