Planta Med 2013; 79(06): 506-512
DOI: 10.1055/s-0032-1328323
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Lupane-Type Triterpenoidal Saponins from Pulsatilla chinensis and Their Anticomplement Activities through the Classical Pathway

Qiong-ming Xu
1   College of Pharmaceutical Science, Soochow University, Suzhou, China
,
Zhan Shu
1   College of Pharmaceutical Science, Soochow University, Suzhou, China
,
Wei-feng Zhu
2   Jiangxi College of Traditional Chinese Medicine, Nanchang, China
,
Yan-li Liu
1   College of Pharmaceutical Science, Soochow University, Suzhou, China
,
Xiao-ran Li
1   College of Pharmaceutical Science, Soochow University, Suzhou, China
,
Shi-lin Yang
1   College of Pharmaceutical Science, Soochow University, Suzhou, China
2   Jiangxi College of Traditional Chinese Medicine, Nanchang, China
› Author Affiliations
Further Information

Publication History

received 26 November 2012
revised 06 February 2013

accepted 08 February 2013

Publication Date:
21 March 2013 (online)

Abstract

Four (14) previously unknown lupane-type triterpenoidal saponins were isolated from the roots of Pulsatilla chinensis, along with six triterpene saponins (510). The structures of saponins 14 were determined as 23-hydroxy-3β-[(O-β-D-glucopyranosyl-(1 → 4)-α-L-arabinopyranosyl)]lup-20(29)-en-28-oic-acid 28-O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl ester (1), 23-hydroxy-3β-[(O-α-L-rhamnopyranosyl-(1 → 2)-[β-D-glucopyranosyl-(1 → 4)]-α-L-arabinopyranosyl)]lup-20(29)-en-28-oic-acid 28-O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl ester (2), 3β-[(O-β-D-glucopyranosyl-(1 → 3)-α-L-rhamnopyranosyl-(1 → 2)-α-L-arabinopyranosyl)]lup-20(29)-en-28-oic-acid 28-O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl ester (3), and 3β-[(O-β-D-glucopyranosyl-(1 → 3)-α-L-rhamnopyranosyl-(1 → 2)-α-L-arabinopyranosyl)]lup-20(29)-en-28-oic-acid 28-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl ester (4), on the basis of hydrolysis and spectral evidence, including 1D- and 2D-NMR and HR-ESI-MS analyses. These pure isolates (110) were tested for their anticomplement activity, using an in vitro assay of the complement system of the classical pathway.

Supporting Information

 
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