A novel multi-target strategy to attenuate the progression of Parkinson's disease by diamine hybrid AGE/ALE inhibitor.

N André Sasaki, Pascal Sonnet

Journal: Future medicinal chemistry 2022;13(24):2185-2200

PMID: 34634921

Abstract

Instead of a conventional 'one-drug-one-target approach', this article presents a novel multi-target approach with a concept of trapping simultaneously as many detrimental factors as possible involved in the progression of Parkinson's disease. These factors include reactive carbonyl species, reactive oxygen species, FeCu and ortho-quinones (-quinone), in particular. Different from the known multi-target strategies for Parkinson's disease, it is a sort of 'vacuum cleaning' strategy. The new agent consists of reactive carbonyl species scavenging moiety and reactive oxygen species scavenging and metal chelating moiety linked by a spacer. Provided that the capacity of scavenging -quinones is demonstrated, this type of agent can further broaden its potential therapeutic profile. In order to support this new hypothetical approach, a number of simple experiments are proposed.

Address: AGIR, UR4294, UFR of Pharmacy, Jules Verne University of Picardie, 80037, Amiens, France.; Centre National de la Recherche Scientifique, 3 Rue Michel Ange, 75016, Paris, France.

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