1. Academic Validation
  2. Antioxidant and Anti-Inflammatory Phenolic Glycosides from Clematis tashiroi

Antioxidant and Anti-Inflammatory Phenolic Glycosides from Clematis tashiroi

  • J Nat Prod. 2015 Jul 24;78(7):1586-92. doi: 10.1021/acs.jnatprod.5b00154.
Li-Jie Zhang 1 Hung-Tse Huang 1 Shih-Yen Huang 2 Zhi-Hu Lin 1 Chien-Chang Shen 1 Wei-Jern Tsai 1 Yao-Haur Kuo 1 3 4
Affiliations

Affiliations

  • 1 †National Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei 112, Taiwan, Republic of China.
  • 2 ‡Endemic Species Research Institute, Nantou County 552, Taiwan, Republic of China.
  • 3 §Graduate Institute of Integrated Medicine, China Medical University, Taichung 404, Taiwan, Republic of China.
  • 4 ⊥Ph.D. Program for the Clinical Drug Discovery from Botanical Herbs, College of Pharmacy, Taipei Medical University, Taipei 110, Taiwan, Republic of China.
Abstract

From the 95% EtOH extract of dried aerial parts of Clematis tashiroi, eight new and four known phenolic (caffeic acid, coumaric acid, ferrulic acid) glycosides were isolated and characterized. The structures of the new isolates (clematisides A-H) were elucidated by spectroscopic data interpretation as trans-4-O-(6-O-trans-caffeoyl-β-D- glucopyranosyl)-9-O-β-D-glucopyranosyl caffeic acid (1), trans-4-O-(6-O-trans-feruloyl-β-D-glucopyranosyll)-9-O-β-D-glucopyranosyl caffeic acid (2), trans-4-O-(6-O-trans-p-coumaroyl-β-D-glucopyranosyl)-9-O-β-D-glucopyranosyl caffeic acid (3), trans-4-O-(6-O-trans-caffeoyl-β-D-glucopyranosyl)-9-O-β-D-glucopyranosyl p-coumaric acid (4), trans-3-O-(6-O-trans-caffeoyl-β-D-glucopyranosyl)-9-O-β-D-glucopyranosyl caffeic acid (5), trans-3-O-(6-O-trans-p-coumaroyl-β-D-glucopyranosyl)-9-O-β-D-glucopyranosyl caffeic acid (6), 6-(3',4'-dihydroxystyryl)-2-pyrone-4-O-(6-O-trans-caffeoyl)-β-D-glucopyranoside (7), and 6-(3',4'-dihydroxystyryl)-2-pyrone-4-O-{6-O-[4-O-(6-O-trans-caffeoyl)-β-D-glucopyranosyl]-trans-caffeoyl}-β-D-glucopyranoside (8), respectively. In a DPPH radical-scavenging test, compounds 1, 7, and 8 showed more potent antioxidant activity than that of the positive control, vitamin E. In addition, compound 7 also showed inhibitory activity in an antinitric oxide release assay.

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