Bolognesi_2009_J.Med.Chem_52_7883

Reference

Title : Toward a rational design of multitarget-directed antioxidants: merging memoquin and lipoic acid molecular frameworks - Bolognesi_2009_J.Med.Chem_52_7883
Author(s) : Bolognesi ML , Cavalli A , Bergamini C , Fato R , Lenaz G , Rosini M , Bartolini M , Andrisano V , Melchiorre C
Ref : Journal of Medicinal Chemistry , 52 :7883 , 2009
Abstract :

Novel multitargeted antioxidants 3-6 were designed by combining the antioxidant features, namely, a benzoquinone fragment and a lipoyl function, of two multifunctional lead candidates. They were then evaluated to determine their profile against Alzheimer's disease. They showed antioxidant activity, improved following enzymatic reduction, in mitochondria and T67 cell line. They also displayed a balanced inhibitory profile against amyloid-beta aggregation and acetylcholinesterase, emerging as promising molecules for neuroprotectant lead discovery.

PubMedSearch : Bolognesi_2009_J.Med.Chem_52_7883
PubMedID: 19813747

Related information

Inhibitor Memoquin

Citations formats

Bolognesi ML, Cavalli A, Bergamini C, Fato R, Lenaz G, Rosini M, Bartolini M, Andrisano V, Melchiorre C (2009)
Toward a rational design of multitarget-directed antioxidants: merging memoquin and lipoic acid molecular frameworks
Journal of Medicinal Chemistry 52 :7883

Bolognesi ML, Cavalli A, Bergamini C, Fato R, Lenaz G, Rosini M, Bartolini M, Andrisano V, Melchiorre C (2009)
Journal of Medicinal Chemistry 52 :7883