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Fitoterapia ; 128: 198-203, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29723564

ABSTRACT

Three triterpene glycosides were isolated from the roots of Weigela florida "rumba" (Bunge) A. DC.: two previously undescribed 3-O-ß-d-xylopyranosyl-(1→2)-[ß-d-xylopyranosyl-(1→4)]-ß-d-xylopyranosyl-(1→4)-ß-d-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-l-arabinopyranosyloleanolic acid (1) and 3-O-ß-d-xylopyranosyl-(1→2)-[ß-d-glucopyranosyl-(1→4)]-ß-d-xylopyranosyl-(1→4)-ß-d-xylopyranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid (2), and one isolated for the first time from a natural source 3-O-ß-d-xylopyranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranosyloleanolic acid (3). Their structures were elucidated mainly by 2D NMR spectroscopic analysis (COSY, TOCSY, NOESY, HSQC, HMBC) and mass spectrometry. Compounds 2 and 3 were further evaluated as antigens in enzyme-linked immunosorbent assay (ELISA) to recognize IgM antibodies in multiple sclerosis (MS) patients' sera.


Subject(s)
Caprifoliaceae/chemistry , Glycosides/isolation & purification , Oleanolic Acid/analogs & derivatives , Plant Roots/chemistry , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin M/chemistry , Molecular Structure , Multiple Sclerosis/blood , Oleanolic Acid/isolation & purification
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