New triterpenoid saponins, maejaposides A, B, C, D, and E, were isolated fr
om the roots of Maesa japonica and were, respectively, defined to be 3-O-[b
eta-D-xylopyranosyl-(1-->2)-alpha-L-rhamnopyranosyl-(1-->2)-beta-D-galactop
yranosyl-(1-->3)] [beta-D-galactopyranosyl-(1-->2)]beta-D-glucuronopyranosi
des of 22 alpha-[(Z)-2-hexenoyloxy]-13 beta,28-oxido-olean-16 alpha,28 alph
a-diol (1); 22 alpha-[2 '-methylbutanoyl]-13 beta,28-oxido-olean-16 alpha,2
8 alpha-diol (2a) and 22 alpha-angeloyloxy-13 beta, 28-oxido-olean-16 alpha
,28 alpha-diol (2b); 21 beta,22 alpha-diangeloyloxy-13 beta,28-oxido-olean-
16 alpha,28 alpha-diol (3); 21 beta-angeloyloxy,22 alpha-(2 '-methylbutanoy
l)-13 beta,28-oxido-olean-16 alpha,28 alpha-diol (4), and 21 beta-angeloylo
xy,22 alpha-[(Z)-2 '-hexenoyl]- 13 beta,28-oxido-olean-16 alpha,28 alpha-di
ol (5). Their structures were established on the basis of extensive NMR (DE
PT, COSY, HOHAHA, HETCOR, HMBC, and NOESY) and ESIMS/MS studies, along with
chemical degradation.