%0 Journal Article %T Hydroxypyridinone-Diamine Hybrids as Potential Neuroprotective Agents in the PC12 Cell-Line Model of Alzheimer's Disease %+ Centre d'Etudes et de Recherche sur le Médicament de Normandie (CERMN) %+ Mécanismes physiopathologiques et conséquences des calcifications vasculaires - UR UPJV 7517 (MP3CV) %+ Agents infectieux, résistance et chimiothérapie - UR UPJV 4294 (AGIR ) %A Lohou, Elodie %A Sasaki, N. Andre %A Boullier, Agnes %A Duplantier, Marine %A Sonnet, Pascal %Z 4th International Electronic Conference on Medicinal Chemistry (ECMC), ELECTR NETWORK, NOV 01-30, 2018 %< avec comité de lecture %@ 1424-8247 %J Pharmaceuticals %I MDPI %V 12 %N 4 %8 2019 %D 2019 %R 10.3390/ph12040162 %Z Life Sciences [q-bio]Journal articles %X There is an urgent need to propose effective treatments for Alzheimer's disease (AD). Although the origin of the disease is poorly understood, several therapeutic options have been proposed. The new therapeutic approaches targeting biometal-mediated neurodegenerative pathways appear to be interesting ones. As a continuation of our preceding studies, two novel series of advanced glycation endproducts (AGE)/advanced lipid peroxidation endproducts (ALE) inhibitors have been developed as multifunctional scavengers. This extended work allowed us to highlight the new hydroxypyridinone-diamine hybrid IIa-3 bearing a C4 alkyl linker between the two pharmacophores. This derivative exhibited preserved potent capacities to trap reactive carbonyl species (vicinal diamine function) as well as reactive oxygen species and transition metals (hydroxypyridinone moiety) in comparison with previously described lead compound 1. In addition, its good predicted absorption, distribution, metabolism and excretion (ADME) properties were correlated with a better efficacy to inhibit in vitro methylglyoxal-induced apoptosis in neuronal-like PC12 cells. This new promising agent revealed improved druglikeness and ability to prevent biometal-mediated oxidative and carbonyl stress amplification involved in AD pathogenesis. %G English %L hal-03568252 %U https://u-picardie.hal.science/hal-03568252 %~ UNIV-PICARDIE %~ COMUE-NORMANDIE %~ UNICAEN %~ CERMN %~ U-PICARDIE %~ MP3CV %~ AGIR-UPJV %~ LABOS-XL-CHEM