New triterpenoid saponins from Maesa japonica

Citation
K. Koike et al., New triterpenoid saponins from Maesa japonica, J NAT PROD, 62(2), 1999, pp. 228-232
Citations number
9
Categorie Soggetti
Agricultural Chemistry","Pharmacology & Toxicology
Journal title
JOURNAL OF NATURAL PRODUCTS
ISSN journal
01633864 → ACNP
Volume
62
Issue
2
Year of publication
1999
Pages
228 - 232
Database
ISI
SICI code
0163-3864(199902)62:2<228:NTSFMJ>2.0.ZU;2-8
Abstract
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.