Camellidin II was isolated as an antifeedant for the larvae of the yellow butterfly, Eurema hecabe mandarina de l'Orza, from the leaves of Camellia japonica L. besides a non-tested camellidin III, identified as its methyl ester, and three inactive known compounds, quinic acid, 3β, 20-dihydroxylupane, and 3, 3', 4-tri-O-methylellagic acid. Spectroscopic and chemical evidence indicates that the structure of camellidin II, reported as an antifungal saponin, is better represented as 3 β, 18 β-dihydroxy-28-norolean-12-en-16-one 3-O-β-D-glucopyranosyl- (1→2) -β-D-galactopyranosyl- (1→3) - [β-D-galactopyranosyl- (1→2)] -β-D-glucuronopyranoside.
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Numata et al. (1987) studied this question.
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