| Literature DB >> 24900356 |
Pablo M Arce1, Omar M Khdour1, Ruth Goldschmidt1, Jeffrey S Armstrong1, Sidney M Hecht1.
Abstract
An aza analogue (1) of the experimental neuroprotective drug idebenone has been prepared and evaluated. The compound quenches lipid peroxidation more effectively than α-tocopherol and potently suppresses reactive oxygen species in cells under oxidative stress. It is thought to do so via a catalytic cycle in which both forms of oxidative stress are suppressed simultaneously. Consequently, the compound effectively protects cultured CEM leukemia cells and Friedreich's ataxia fibroblasts from oxidative stress more effectively than idebenone or idebenol.Entities:
Keywords: Reactive oxygen species; electron transport chain; lipid peroxidation; mitochondria
Year: 2011 PMID: 24900356 PMCID: PMC4018135 DOI: 10.1021/ml200095w
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345