
Constituintes químicos de Parmotrema lichexanthonicum Eliasaro & Adler: isolamento, modificações estruturais e avaliação das atividades antibiótica e citotóxica
2009; Brazilian Chemical Society; Volume: 32; Issue: 1 Linguagem: Inglês
10.1590/s0100-40422009000100003
ISSN1678-7064
AutoresAna Camila Micheletti, Adilson Beatriz, Dênis Pires de Lima, N Honda, Cláudia Pessoa, Manoel Odorico de Moraes, Letícia V. Costa‐Lotufo, Hemerson Iury Ferreira Magalhães, Nádia Cristina Pereira Carvalho,
Tópico(s)Cancer Treatment and Pharmacology
ResumoANTIBIOTIC AND CYTOTOXIC ACTIVITIES.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.
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