Three new cardenolide glycosides were isolated from the seeds of Cotchorus olitorius L. On the basis of chemical and spectroscopic evidence, their structures were established as cannogenol 3-O-β-D-glucopyranosyl-(1 → 4)-O-β-D-boivinopyranoside, periplogenin 3-O-β-D-glucopyranosyl-(1 → 4)- O-β-D-digitoxopyranoside and digitoxigenin 3-O-β-D-glucopyranosyl-(1 → 6)- O-β-D-glucopyranosyl-(1 → 4)-O-β-D-digitoxopyranoside.
NMR, Corchorus olitorius, Tiliaceae, boivinose, cannogenol, cardenolide glycoside, digitoxigenin, digitoxose, periplogenin, tossa jute
NCBI PubMed ID: 9883596Publication DOI: 10.1016/S0031-9422(98)00421-XJournal NLM ID: 0151434Publisher: Elsevier
Institutions: National Institute of Health Sciences, Setagaya, Tokyo, Japan
Methods: 13C NMR, 1H NMR, FAB-MS, extraction, optical rotation measurement, CD, HMQC, COSY, MPLC, HR-FAB-MS