Fractionation of an aqueous acetone extract of the whole herb of Genti
ana algida gave one new [2'(o,m-dihydroxybenzyl)sweroside] and five kn
own secoiridoids, together with anofinic acid, fomannoxin acid, sitost
erol, daucosterol, stigmasterol, oleanolic acid, orientin and gentiano
se. The structures were determined by spectral methods and a few chemi
cal transformations. Anofinic acid and fomannoxin acid were found to b
e active against Cladosporium cucumerinum, a plant pathogenic fungus.
Preliminary structure-activity studies indicated that the presence of
carboxylic moieties in these acids was presumably a precondition for a
ctivity, whereas their methyl esters, inactive to the fungus, were act
ive against the human pathogenic yeast Candida albicans. The chemotaxo
nomic significance of the isolates is discussed briefly.