Superheated water chromatography-nuclear magnetic resonance spectroscopy of kava lactones.
Orapin Chienthavorn, Roger M Smith, Ian D Wilson, Brian Wright, Eva M Lenz
Index: Phytochem. Anal. 16(3) , 217-21, (2005)
Full Text: HTML
Abstract
Three kava lactone constituents of Piper methysticum, namely, kawain, methysticin and desmethoxyyangonin, have been separated and identified by reversed-phase HPLC using superheated deuterium oxide as the mobile phase and on-line 1H-NMR detection. The method avoids the use of organic solvents in the mobile phase and hence interferences in the NMR analysis are minimised.
Related Compounds
Related Articles:
Fatal kavalactone intoxication by suicidal intravenous injection.
2015-04-01
[Forensic Sci. Int. 249 , e7-11, (2015)]
Interaction of various Piper methysticum cultivars with CNS receptors in vitro.
2001-06-01
[Planta Med. 67(4) , 306-11, (2001)]
Kavalactones fail to inhibit alcohol dehydrogenase in vitro.
2006-02-01
[Phytomedicine 13(3) , 192-5, (2006)]
In vitro toxicity of kava alkaloid, pipermethystine, in HepG2 cells compared to kavalactones.
2004-05-01
[Toxicol. Sci. 79(1) , 106-11, (2004)]
Kavalactones Yangonin and Methysticin induce apoptosis in human hepatocytes (HepG2) in vitro.
2011-03-01
[Phytother Res. 25(3) , 417-23, (2011)]