Autor(es)Ee G C L,Daud S,Taufiq-Yap Y H,Ismail N H,Rahmani M

ResumoStudies on the stem of Garcinia mangostana have led to the isolation of one new xanthone mangosharin (1) (2,6-dihydroxy-8-methoxy-5-(3-methylbut-2-enyl)-xanthone) and six other prenylated xanthones, alpha-mangostin (2), beta-mangostin (3), garcinone D (4), 1,6-dihydroxy-3,7-dimethoxy-2-(3-methylbut-2-enyl)-xanthone (5), mangostanol (6) and 5,9-dihydroxy-8- methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-2H,6H-pyrano-[3,2-b]-xanthene-6-one (7). The structures of these compounds were determined by spectroscopic methods such as 1H NMR, 13C NMR, mass spectrometry (MS) and by comparison with previous studies. All the crude extracts when screened for their larvicidal activities indicated very good toxicity against the larvae of Aedes aegypti. This article reports the isolation and identification of the above compounds as well as bioassay data for the crude extracts. These bioassay data have not been reported before.

Palavras-ChaveGarcinia mangostana; Xanthones; Larvicidal; Aedes aegypti

ImprentaNatural Product Research, v. 20, n. 12, p. 1067-1073, 2006

DescritoresAedes aegypti - Molecular Structure ; Aedes aegypti - Molecular methods

Data de Publicação:2006