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Planta Med 2012; 78(12): 1391-1394
DOI: 10.1055/s-0032-1314980
Natural Product Chemistry
Letters
Georg Thieme Verlag KG Stuttgart · New York

Cycloartane-type Triterpene Glycosides from the Rhizomes of Cimicifuga heracleifolia and Their Anticomplementary Activity

Jung Hoon Lee   *
1   College of Pharmacy, Catholic University of Daegu, Gyeongbuk, Korea
,
To Dao Cuong   *
1   College of Pharmacy, Catholic University of Daegu, Gyeongbuk, Korea
,
Seung Jun Kwack
2   College of Natural Science, Changwon National University, Kyeongnam, Korea
,
Ji Hyeon Seok
2   College of Natural Science, Changwon National University, Kyeongnam, Korea
,
Jong Kwon Lee
3   Toxicology Evaluation and Research Department, Korea Food & Drug Administration, Chungbuk, Korea
,
Ja Young Jeong
3   Toxicology Evaluation and Research Department, Korea Food & Drug Administration, Chungbuk, Korea
,
Mi-Hee Woo
1   College of Pharmacy, Catholic University of Daegu, Gyeongbuk, Korea
,
Jae Sue Choi
4   Faculty of Food Science and Biotechnology, Pukyoung National University, Busan, Korea
,
Hyeong Kyu Lee
5   Natural Medicine Research Center, KRIBB, Chungbuk, Korea
,
Byung Sun Min
1   College of Pharmacy, Catholic University of Daegu, Gyeongbuk, Korea
6   Advanced Medical Research Center, Catholic University of Daegu, Gyeongbuk, Korea
› Author Affiliations
Further Information

Publication History

received 16 March 2012
revised 25 May 2012

accepted 27 May 2012

Publication Date:
29 June 2012 (online)

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Abstract

Seven known triterpene glycosides, 23-O-acetylshengmanol 3-O-α-L-arabinopyranoside (1), 23-O-acetylshengmanol 3-O-β-D-xylopyranoside (2), 24-epi-24-O-acetylhydroshengmanol 3-O-β-D-xylopyranoside (3), cimiaceroside B (4), (23R,24S)-cimigenol 3-O-β-D-xylopyranoside (5), (23R,24R)-25-O-acetylcimigenol 3-O-β-D-xylopyranoside (6) and (23R,24S)-25-O-anhydrocimigenol 3-O-β-D-xylopyranoside (7) were isolated from the rhizomes of Cimicifuga heracleifolia. Their chemical structures were determined on the basis of spectroscopic analyses including 2D NMR. All isolates were investigated for their inhibitory effects on the classical pathway of the complement system. Among them, compound 6 showed strong inhibitory activity with an IC50 value of 7.7 µM while compound 3 was moderately active with an IC50 value of 195.6 µM.

Key words

Cimicifuga heracleifolia - Ranunculaceae - cycloartane glycoside - anticomplement activity

* These authors contributed equally to this work.


 

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