1. Academic Validation
  2. Cycloartane-type triterpene glycosides from the rhizomes of Cimicifuga heracleifolia and their anticomplementary activity

Cycloartane-type triterpene glycosides from the rhizomes of Cimicifuga heracleifolia and their anticomplementary activity

  • Planta Med. 2012 Aug;78(12):1391-4. doi: 10.1055/s-0032-1314980.
Jung Hoon Lee 1 To Dao Cuong Seung Jun Kwack Ji Hyeon Seok Jong Kwon Lee Ja Young Jeong Mi-Hee Woo Jae Sue Choi Hyeong Kyu Lee Byung Sun Min
Affiliations

Affiliation

  • 1 College of Pharmacy, Catholic University of Daegu, Gyeongbuk, Korea.
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.

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