Bioactive Sesquiterpene Lactones Isolated from the Whole Plants of Vernonia cinerea
- J Nat Prod. 2019 Aug 23;82(8):2124-2131. doi: 10.1021/acs.jnatprod.8b01078.
- 1. Department of Pharmaceutical Sciences, Daniel K. Inouye College of Pharmacy , University of Hawai'i at Hilo , Hilo , Hawaii 96720 , United States.
- 2. Department of Pharmacy , Renmin Hospital of Wuhan University , Wuhan 430060 , People's Republic of China.
- 3. Department of Biological Sciences , Clemson University , Clemson , South Carolina 29634 , United States.
- 4. Daniel K. Inouye U.S. Pacific Basin Agricultural Research Center , USDA-ARS, Hilo , Hawaii 96720 , United States.
- 5. Department of Pharmacognosy, Faculty of Pharmacy , Rangsit University , Pathum Thani 12000 , Thailand.
- 6. Department of Pharmacy Practice, Daniel K. Inouye College of Pharmacy , University of Hawai'i at Hilo , Hilo , Hawaii 96720 , United States.
Twelve sesquiterpene lactones were isolated from the whole Plants of Vernonia cinerea. These included eight new compounds, vercinolides A-H (1-8), along with four known substances (9-12). The structures of the new compounds were determined by 1D and 2D NMR experiments and mass spectrometric methods. The absolute configurations of compounds 1-8 were determined by Mosher experiments and ECD data. Compounds 1-8 are the first examples of a new class of sesquiterpene lactones possessing a rare 4α,10α-ether ring and a 2,14-ether ring. Compounds 1-4, 6, 8, 10, and 12 were evaluated for their cytotoxic and anti-inflammatory activities. Compounds 10 and 12 exhibited inhibitory effects against nitric oxide production in lipopolysaccharide-activated RAW 264.7 mouse macrophage cells with IC50 values of 21 and 23 μM, respectively. Both compounds were inactive for HeLa cells (IC50 > 10 μM).