Efficient Catalytic Oxidation of 3-Arylthio- and 3-Cyclohexylthio-lapachone Derivatives to New Sulfonyl Derivatives and Evaluation of Their Antibacterial Activities

New sulfonyl-lapachones were efficiently obtained through the catalytic oxidation of arylthio- and cyclohexylthio-lapachone derivatives with hydrogen peroxide in the presence of a Mn(III) porphyrin complex. The antibacterial activities of the non-oxidized and oxidized lapachone derivatives against t...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2017-02, Vol.22 (2), p.302-302
Hauptverfasser: Cardoso, Mariana F do C, Gomes, Ana T P C, Moreira, Caroline Dos S, Simões, Mário M Q, Neves, Maria G P M S, da Rocha, David R, da Silva, Fernando de C, Moreirinha, Catarina, Almeida, Adelaide, Ferreira, Vitor F, Cavaleiro, José A S
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Sprache:eng
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Zusammenfassung:New sulfonyl-lapachones were efficiently obtained through the catalytic oxidation of arylthio- and cyclohexylthio-lapachone derivatives with hydrogen peroxide in the presence of a Mn(III) porphyrin complex. The antibacterial activities of the non-oxidized and oxidized lapachone derivatives against the Gram-negative bacteria and the Gram-positive bacteria were evaluated after their incorporation into polyvinylpyrrolidone (PVP) micelles. The obtained results show that the PVP-formulations of the lapachones - and of the sulfonyl-lapachones and reduced the growth of .
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules22020302