Resumo

MICHELETTI, Ana C. et al. Chemical constituents of parmotrema lichexanthonicum Eliasaro & Adler: isolation, structure modification and evaluation of antibiotic and cytotoxic activities. Quím. Nova [online]. 2009, vol.32, n.1, pp. 12-20. ISSN 0100-4042.  http://dx.doi.org/10.1590/S0100-40422009000100003.

From the lichen Parmotrema lichexantonicum were isolated the depsidone salazinic acid, the xanthone lichexanthone, and the depside atranorin. The two major compounds, salazinic acid and lichexanthone, were selected for structure modifications. Salazinic acid afforded O-alkyl salazinic acids, some of them potentially cytotoxic against tumor cell lines (HCT-8, SF-295 and MDA/ MB - 435). From lichexanthone were 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 and 3,6-bis[3-(dimethylamine)propoxy]-1-hydroxy-8-methyl-9H-xanten-9-one. The last compound was the most active against S. aureus.

Palavras-chave : lichexanthone; salazinic acid; lichens.