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Cytotoxic triterpene glycosides from the roots of Sanguisorba officinalis

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Abstract

Phytochemical investigation of the ethanol extract of the roots of Sanguisorba officinalis resulted in the isolation of three new triterpene glycosides, 3β-[(α-L-arabinopyranosyl)oxy]-19α,23-dihydroxyolean-12-en-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (1), 2α,3β,19α,23-tetrahydroxyurs-12-en-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (2), and 3β-[(α-L-arabinopyranosyl)oxy]-19α-hydroxyurs-12,20(30)-dien-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (3). All the triterpene glycosides exhibited the significant cytotoxic potential with low IC50 values (IC50 < 5.0 μM) against six tumor cell lines (MCF-7, HeLa, HepG2, SGC-7901, NCI-H460, and BGC-823).

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Acknowledgments

The above research was made possible by the grant from the Scientific Planning Project of the Applied Basic Research of Yunnan Province (S2012FZ0005) and the Developing Key Subject of Ecology of Qujing Normal University.

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Correspondence to Jiang Hu.

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Jiang Hu and Yan Song have contributed equally to this work.

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Hu, J., Song, Y., Li, H. et al. Cytotoxic triterpene glycosides from the roots of Sanguisorba officinalis . Arch. Pharm. Res. 38, 984–990 (2015). https://doi.org/10.1007/s12272-014-0477-3

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  • DOI: https://doi.org/10.1007/s12272-014-0477-3

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