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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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

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 1 microM concentration, reduced reperfusion arrhythmias and MDA content on isolated rat heart preparations, with the 2- and 5-subtituted chromans possessing the better cardioprotective activity.[1]

References

  1. Synthesis of chroman analogues of lipoic acid and evaluation of their activity against reperfusion arrhythmias. Koufaki, M., Detsi, A., Theodorou, E., Kiziridi, C., Calogeropoulou, T., Vassilopoulos, A., Kourounakis, A.P., Rekka, E., Kourounakis, P.N., Gaitanaki, C., Papazafiri, P. Bioorg. Med. Chem. (2004) [Pubmed]
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