Synthesis of chroman analogues of lipoic acid and evaluation of their activity against reperfusion arrhythmias

[Display omitted] Novel hybrids of lipoic acid and trolox connected through triamine spacers as well as analogues in which the lipoic acid was attached at different positions of the chroman moiety of vitamin E through an amide bond, were synthesized and exhibited strong inhibition of the microsomal...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2004-09, Vol.12 (18), p.4835-4841
Hauptverfasser: Koufaki, Maria, Detsi, Anastasia, Theodorou, Elissavet, Kiziridi, Christina, Calogeropoulou, Theodora, Vassilopoulos, Athanasios, Kourounakis, Angeliki P., Rekka, Eleni, Kourounakis, Panos N., Gaitanaki, Catherine, Papazafiri, Panagiota
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Sprache:eng
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Zusammenfassung:[Display omitted] Novel hybrids of lipoic acid and trolox connected through triamine spacers as well as analogues in which the lipoic acid was attached at different positions of the chroman moiety of vitamin E through an amide bond, were synthesized and exhibited strong inhibition of the microsomal lipid peroxidation. Moreover, the new molecules, at 1μM concentration, reduced reperfusion arrhythmias and MDA content on isolated rat heart preparations, with the 2- and 5-subtituted chromans possessing the better cardioprotective activity.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2004.07.012