
To find new active constituents from Rhizome of Cimicifuga foetida.Various column chromatographic techniques were employed for isolation and purification. The structures were elucidated on the basis of spectral and chemical evidences.Four triterpenoid compounds were isolated and identified as 7,8-didehydro-27-deoxyactein(1), 24-O-acetylshengmanol-3-O-beta-D-xyl (23R, 24R)[2], cimigenol(3), cimigenol-3-O-beta-D-xyl(4).Compound 1 is a new compound, 2-4 were obtained from this medicinal material for the first time. The antiosteoporosis activity screening in vitro(by the method of SRB) indicates that Compounds 1, 2 and 4 can promote the proliferation for rat Osteoblastoma cell line (UMR106) at the concentration of 10(-9) kg.L-1.
Cimicifuga, Plants, Medicinal, Molecular Structure, Bone Neoplasms, Triterpenes, Rats, Lanosterol, Cell Line, Tumor, Animals, Osteoblastoma, Cell Division, Rhizome
Cimicifuga, Plants, Medicinal, Molecular Structure, Bone Neoplasms, Triterpenes, Rats, Lanosterol, Cell Line, Tumor, Animals, Osteoblastoma, Cell Division, Rhizome
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