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Synthesis of triphenylphosphonium vitamin E derivatives as mitochondria-targeted antioxidants.
Jameson, Victoria J A; Cochemé, Helena M; Logan, Angela; Hanton, Lyall R; Smith, Robin A J; Murphy, Michael P.
Afiliação
  • Jameson VJ; Department of Chemistry, University of Otago, PO Box 56, Dunedin, 9054, New Zealand.
  • Cochemé HM; MRC Clinical Sciences Centre, Imperial College, London, W12 0NN, UK ; MRC Mitochondrial Biology Unit, Hills Road, Cambridge, CB2 0XY, UK.
  • Logan A; MRC Mitochondrial Biology Unit, Hills Road, Cambridge, CB2 0XY, UK.
  • Hanton LR; Department of Chemistry, University of Otago, PO Box 56, Dunedin, 9054, New Zealand.
  • Smith RA; Department of Chemistry, University of Otago, PO Box 56, Dunedin, 9054, New Zealand.
  • Murphy MP; MRC Mitochondrial Biology Unit, Hills Road, Cambridge, CB2 0XY, UK.
Tetrahedron ; 71(44): 8444-8453, 2015 Nov 04.
Article em En | MEDLINE | ID: mdl-26549895
ABSTRACT
A series of mitochondria-targeted antioxidants comprising a lipophilic triphenylphosphonium cation attached to the antioxidant chroman moiety of vitamin E by an alkyl linker have been prepared. The synthesis of a series of mitochondria-targeted vitamin E derivatives with a range of alkyl linkers gave compounds of different hydrophobicities. This work will enable the dependence of antioxidant defence on hydrophobicity to be determined in vivo.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article