Sh. Park et al., Anticomplement activities of oleanolic acid monodesmosides and bisdesmosides isolated from Tiarella polyphylla, ARCH PH RES, 22(4), 1999, pp. 428-431
Seven known oleanolic acid glycosides (1-7) were isolated from the MeOH ext
ract of Tiarella polyphylla. The structures were identified to be 3-O-(beta
-D-glucopyranosyl) oleanolic acid (1), 3-O-[beta-D-glucopyranosyl-(1 --> 3)
-beta-D-glucopyranosyl] oleanolic acid (2), 3-O-[beta-D-glucopyranosyl- (1
--> 2)-beta-D-glucopyranosyl] oleanolic acid (3), 3-O-[beta-D-glucopyranosy
l-(1 --> 3)-beta-D-glucopyranosyl] oleanolic acid 28-O-beta-D-glucopyranosy
l eater (4), 3-O-[beta-D-glucopyranosyl-(1 --> 2)-beta-D-glucopyranosyl] ol
eanolic acid 28-O-beta-D-glucopyranosyl ester (5), 3-O-[a-L-rhamnopyranosyl
-(1 --> 3)-beta-D-glucuronopyranosyl] oleanolic acid (6), and 3-O-[alpha-L-
rhamnopyranosyl-(1 --> 3)-beta-D-glucuronopyranosyl] oleanolic acid 28-O-be
ta-D-glucopyranosyl ester (7) on the basis of physicochemical and spectral
data. These triterpene glycosides were tested for the anticomplement activi
ty and hemolytic activity. Bisdesmosidic saponins, 4, 5, and 7, showed anti
complement activity; in contrast, monodesmosidic saponins, 1-3, and 6, show
ed direct hemolytic activity Methyl esterified monodesmosidic saponins show
ed anticomplement activity at a low concentration and hemolytic activity at
a high concentration.