Repeated fractionation of an aqueous ethanol extract of the whole herb
of Wahlenbergia marginata afforded six ionone-related and five phenyl
propanoid-derived glycosides. The structures of the five new compounds
were established by spectroscopic and chemical methods as ta-D-glucop
yranosyloxy)ethyl-cyclohexa-2-en-l-one, demethyl syringin, wahlenoside
s A, B and C, respectively. All constituents were not active against t
he human pathogenic fungi Candida albican, Trichoderma viride and Aspe
rgillus flavus. (C) 1998 Elsevier Science Ltd. All rights reserved.