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Ypsilandrosides C-G, five new spirostanol saponins from Ypsilandra thibetica
- Source :
- Steroids. 74:950-955
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- A further phytochemical investigation on the whole plants of Ypsilandra thibetica yielded one sapogenin and 12 spirostanol saponins. Five of these are new compounds, designated as ypsilandrosides C-G (2-6). Their structures were determined by detailed spectroscopic analysis, including extensive 1D and 2D NMR data, and by the result of a hydrolytic reaction. Compounds 2-5 were rare steroidal saponins that an apiofuranosyl unit was directly linked at C-3 of the aglycone. Selected spirostanol saponins (2-6, 9) were tested for their cytotoxic activities against K562, SPC-A-1, BGC-823, Eca-109, and AGS cell lines. Compounds 6 and 9 showed moderate inhibitory activity against all five cell lines. The antifungal properties of the new spirostanol saponins (2-6) against Candida albicans were also determined. (C) 2009 Elsevier Inc. All rights reserved.
- Subjects :
- Antifungal Agents
Stereochemistry
Chemical structure
Clinical Biochemistry
Antineoplastic Agents
Sapogenin
Biochemistry
Magnoliopsida
chemistry.chemical_compound
Endocrinology
Cell Line, Tumor
Candida albicans
Ypsilandra thibetica
Spirostans
Humans
Molecular Biology
Pharmacology
biology
Liliaceae
Organic Chemistry
Saponins
biology.organism_classification
Aglycone
chemistry
Phytochemical
Two-dimensional nuclear magnetic resonance spectroscopy
Subjects
Details
- ISSN :
- 0039128X
- Volume :
- 74
- Database :
- OpenAIRE
- Journal :
- Steroids
- Accession number :
- edsair.doi.dedup.....2ef25a99650e9f2cd457f1ad94bcc718
- Full Text :
- https://doi.org/10.1016/j.steroids.2009.07.001