作者: Ana C Micheletti , Adilson Beatriz , Dênis Pires de Lima , Neli K Honda , Cláudia do Ó Pessoa
DOI: 10.1590/S0100-40422009000100003
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摘要: From the lichen Parmotrema lichexantonicum were isolated depsidone salazinic acid, xanthone lichexanthone, and depside atranorin. The two major compounds, acid selected for structure modifications. Salazinic afforded O-alkyl acids, some of them potentially cytotoxic against tumor cell lines (HCT-8, SF-295 MDA/ MB - 435). lichexanthone obtained norlichexanthone, 3-O-methylnorlichexanthone, 3-O-methyl-6-O-prenylnorlichexanthone, 3,6-di-O-prenyl-norlichexanthone, 3,6-bis[(3,3-dimethyloxyran-2-il)methoxy]-1-hydroxy-8-methyl-9H-xanten-9-one 3,6-bis[3-(dimethylamine)propoxy]-1-hydroxy-8-methyl-9H-xanten-9-one. last compound was most active S. aureus.