A new ginsengenin containing an oxacyclopentane-ring isolated from the acid hydrolysate of total ginsenosides
Bioassay-guided fractionation of the acid hydrolysate of total ginsenosides of Panax ginseng C.A.Meyer (Araliaceae) led to the isolation of a novel ginsengenin(1).The structure of 1 was determined as (20S,22S)-dammar-22,25-epoxy-3β,12β,20-triol by extensive spectroscopy and single-crystal X-ray diff...
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Veröffentlicht in: | Chinese chemical letters 2013-06, Vol.24 (6), p.524-526 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bioassay-guided fractionation of the acid hydrolysate of total ginsenosides of Panax ginseng C.A.Meyer (Araliaceae) led to the isolation of a novel ginsengenin(1).The structure of 1 was determined as (20S,22S)-dammar-22,25-epoxy-3β,12β,20-triol by extensive spectroscopy and single-crystal X-ray diffraction analyses.The cytotoxicity of 1 was further tested against SWl 116,HCTl 16,and A549 cells by the MTT method,with IC50 values in the range of 2.96-30.9μmol/L. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2013.03.044 |