| Literature DB >> 27603739 |
José-Luis Giner1, Ju Feng1, David J Kiemle1.
Abstract
The sugar subunits of natural glycosides can be conveniently determined by acid hydrolysis and (1)H NMR spectroscopy without isolation or derivatization. The chemical shifts, coupling constants, and integral ratios of the anomeric signals allow each monosaccharide to be identified and its molar ratio to other monosaccharides to be quantified. The NMR data for the anomeric signals of 28 monosaccharides and three disaccharides are reported. Application of the method is demonstrated with the flavonoid glycoside naringin (1), the aminoglycoside antibiotics kanamycin (2) and tobramycin (3), and the saponin digitonin (4).Entities:
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Year: 2016 PMID: 27603739 DOI: 10.1021/acs.jnatprod.6b00180
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050