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. 2009 Apr 17;14(4):1578-84.
doi: 10.3390/molecules14041578.

Trinor-cycloartane glycosides from the rhizomes of Cimicifuga foetida

Lu Lu  1 , Jianchao Chen, Yin Nian, Yun Sun, Minghua Qiu
Affiliations

Trinor-cycloartane glycosides from the rhizomes of Cimicifuga foetida

Lu Lu et al. Molecules. .

Abstract

Three new trinor-cycloartane glycosides, 15alpha-hydroxy-16-dehydroxy-16(24)-en-foetidinol-3-O-beta-D-xylopyranoside (1), 28-hydroxy-foetidinol-3-O-beta-D-xylopyranoside (2) and foetidinol-3-O-beta-D-xylopyranosyl-(1"-->3')-beta-D-xylopyranoside (3) together with the known compound foetidinol-3-O-beta-D-xylopyranoside (4) were isolated from the n-BuOH fraction of the roots of Cimicifuga foetida. Their structures were elucidated on the basis of spectroscopic and chemical reaction data.

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Figures

Figure 1
Figure 1
Structures of compounds 1, 2 and 3.
Figure 2
Figure 2
HMBC correlations of compounds 1 and 2.
Figure 3
Figure 3
HMBC correlations of the disaccharide in compound 3.
See this image and copyright information in PMC

References

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