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. Author manuscript; available in PMC: 2009 Jun 1.
Published in final edited form as: Phytomedicine. 2007 Nov 5;15(6-7):504–511. doi: 10.1016/j.phymed.2007.09.017

Table 2.

Effect of purified triterpene glycosides/aglycone from Cimicifuga species on cell proliferation in MDA-MB-453 (Her2 overexpressing) human breast cancer cells

Code Plant Species Chemical Name M.W. IC50 µg/ml IC50 µM
A1 Cimicifuga acerina Cimigenol 3-O-β-D-xylopyranoside 620 6 9.7
C2 Cimicifuga acerina (22R)-22-hydroxycimigenol 3-O-β-D-xylopyranoside 636 29 45.6
d6 Cimicifuga dahurica 24-epi-7,8-didehydrocimigenol 3-O-β-D-xylpyranoside 618 7.2 11.7
d8 Cimicifuga dahurica 12 β-hydroxycimigenol 3-O-α-L-arabinopyranoside 636 55 86.5
d10 Cimicifuga dahurica 24-O-acetylisodahurinol 3-O-α-L-arabinopyranoside 684 17 24.9
d11 Cimicifuga dahurica 7,8-didehydrocimigenol 3-O-β-D-xylopyranoside 596 7.2 12.1
d13 Cimicifuga acerina 25-acetyl-7,8-didehydrocimigenol 3-O-β-D-xylopyranoside 638 3.2 5.0
dE Cimicifuga dahurica 3-O-α-L-arabinopyranosyl cimigenol 15-O-β-D-glucopyranoside 804 72 89.6
Ac Actaea racemosa actein, β-D-xylopyranoside 676 5.7 8.4

MDA-MB-453 cells were treated with increasing concentrations of each of the Cimicifuga components for 96 h and the number of viable cells determined using a Coulter Counter. Similar results were obtained in an additional study.

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