Abstract
The rhizomes of Convallaria majalis have been analyzed for their steroidal glycoside constituents, resulting in the isolation of a new 5beta-spirostanol triglycoside, named convallasaponin A, along with two known cardenolide glycosides and a known cholestane glycoside. The structure of convallasaponin A was determined on the basis of extensive spectroscopic analysis, including 2D NMR data, and the results of hydrolytic cleavage. The cardenolide glycosides showed tumor specific cytotoxic activity.
MeSH terms
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Antineoplastic Agents, Phytogenic / chemistry
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Antineoplastic Agents, Phytogenic / isolation & purification*
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Antineoplastic Agents, Phytogenic / pharmacology
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Convallaria / chemistry*
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Glycosides / chemistry*
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Glycosides / isolation & purification
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Glycosides / pharmacology
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Humans
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Hydrolysis
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Magnetic Resonance Spectroscopy
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Molecular Structure
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Plants, Medicinal / chemistry*
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Spirostans / chemistry*
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Spirostans / isolation & purification
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Spirostans / pharmacology
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Tumor Cells, Cultured / drug effects
Substances
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Antineoplastic Agents, Phytogenic
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Glycosides
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Spirostans
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convallasaponin A