Tham khảo Kavain

  1. ↑ Bradić, I; Pasini, M (1975). “Hirschsprung's disease -- therapy and results”. Acta Chirurgica Iugoslavica. 22 (2): 183–95. PMID 1235738.
  2. ↑ Boonen, Georg; Häberlein, Hans (2007). “Influence of Genuine Kavapyrone Enantiomers on the GABAABinding Site”. Planta Medica. 64 (6): 504–6. doi:10.1055/s-2006-957502. PMID 9776662.
  3. ↑ Chua HC, Christensen ET, Hoestgaard-Jensen K, Hartiadi LY, Ramzan I, Jensen AA, Absalom NL, Chebib M (2016). “Kavain, the Major Constituent of the Anxiolytic Kava Extract, Potentiates GABAA Receptors: Functional Characteristics and Molecular Mechanism”. PLoS ONE. 11 (6): e0157700. doi:10.1371/journal.pone.0157700. PMC 4917254. PMID 27332705.
  4. ↑ Grunze, Heinz; Langosch, Jens; Schirrmacher, Karin; Bingmann, Dieter; Von Wegerer, Jörg; Walden, Jörg (2001). “Kava pyrones exert effects on neuronal transmission and transmembraneous cation currents similar to established mood stabilizers - a review”. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 25 (8): 1555–70. doi:10.1016/S0278-5846(01)00208-1. PMID 11642654.
  5. ↑ Rowe, A.; Narlawar, R.; w. Groundwater, P.; Ramzan, I. (2011). “Kavalactone Pharmacophores for Major Cellular Drug Targets”. Mini Reviews in Medicinal Chemistry. 11 (1): 79–83. doi:10.2174/138955711793564088. PMID 21034404.