| Literature DB >> 10346954 |
X M Du1, N Y Sun, M Nishi, T Kawasaki, Y T Guo, K Miyahara.
Abstract
An ether-insoluble resin glycoside fraction was obtained from the seeds of Cuscuta australis. Identification and characterization of alkaline hydrolysis products by means of GC, FABMS, and 1H, 13C, and 2D NMR revealed the material to be composed of three new glycosidic acids, cuscutic acids A1-A3 (1-3); triglycosides with (11S)-jalapinolic or (11S)-convolvulinolic acid as the aglycon; and acetic, isobutyric, (2S)-2-methylbutyric, tiglic, and (2R,3R)-nilic acids. The resin glycoside is considered to be a complex mixture of glycosidic ester-type oligomers (up to heptamers) with a core consisting of a number of the above cuscutic acids each acylated with one or two carboxylic acid moieties.Entities:
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Year: 1999 PMID: 10346954 DOI: 10.1021/np980506j
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050