Abstract
Two new triterpene glycosides, coryternic acid 3-O - D-glucuronopyranoside (1) and coryternic acid 3-O - D-glucuronopyranoside-6-O-methyl ester (2), were isolated from a MeOH extract of the tubers of Corydalis ternata. Acidic hydrolysis of 1 and 2 yielded a new triterpene as their aglycone, coryternic acid (3). The structures of these new compounds were determined through spectral analysis, including extensive 2D-NMR data. In this study we reported that triterpenoids were first isolated from the genus Corydalis. Compound 2 exhibited significant cytotoxicity against the A549, SK-OV-3, SK-MEL-2, and HCT-15 cell lines (IC15.16, 17.07, 13.32, and 11.95M, respectively) and significantly reduced NO production in lipopolysaccharide (LPS)-activated microglia/BV-2 cells with an ICvalue of 16.2M without cell toxicity.
| Original language | English |
|---|---|
| Pages (from-to) | 1555-1558 |
| Number of pages | 4 |
| Journal | Planta Medica |
| Volume | 77 |
| Issue number | 13 |
| DOIs | |
| State | Published - 2011 |
Keywords
- Corydalis ternate
- cytotoxicity
- neuroinflammation
- Papaveraceae
- triterpenes
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