About: Santonin is a research topic. Over the lifetime, 153 publications have been published within this topic receiving 865 citations. The topic is also known as: (-)-alpha-Santonin & (-)-Santonin.
TL;DR: Parthenolide, costunolide and santonin were able to rescue planaria from C-like hyperkinesia, after the worms were exposed to cocaine, which suggests a common binding site for cocaine and the sesquiterpene lactones in planarians.
Abstract: Here we report the prevention and reversal of cocaine-induced behaviors in planarian worms by parthenolide and two related cyclic sesquiterpene lactones (SL), costunolide and santonin. Using established protocols, we studied two cocaine-induced behavioral effects in planaria; the induction of motility decrease and the induction of C-like hyperkinesia. Cocaine, parthenolide, costunolide, santonin, and a lactone-less cyclic sesquiterpene, β-eudesmol, decreased planarian motility in a concentration-dependent manner. Only cocaine induced C-like hyperkinesia. At concentrations that did not show any motility decrease, partenolide, costunolide and santonin, but not β-eudesmol, significantly reduced the cocaine-induced motility decrease and C-like hyperkinesia, in a concentration-dependent manner. Furthermore, partenolide, costunolide and santonin were able to rescue planaria from C-like hyperkinesia, after the worms were exposed to cocaine. Conversely, cocaine at a concentration that did not show any measurable effects (10 µM), was able to alleviate the SL-, but not the β-eudesmol-induced motility decrease. Liquid Chromatography/Mass Spectrometry experiments demonstrated that cocaine does not interact directly with any of the cyclic sesquiterpenoids, which suggests specific biochemical targets for these compounds in planarians. Our data suggests a common binding site for cocaine and the sesquiterpene lactones in planarians.
TL;DR: The photochemistry of santonin has an illustrious history which has dealt, in the main, with the isolation, characterisation, and interrelation of the manifold products formed on exposure of Santonin to light in various media as mentioned in this paper.
Abstract: The photochemistry of santonin has an illustrious
history which has dealt, in the main, with the isolation,
characterization, and interrelation of the manifold
products formed on exposure of santonin to light in
various media. The established course of the reaction
in certain media is from santonin (I) to lumisantonin
(II) and thence to photosantonic acid (IV).
TL;DR: Santonin, a sesquiterpene lactone, commonly found in the plants of the family Compositae was found to show significant antiinflammatory activity on acute inflammatory processes and caused a significant antipyretic effect in mice.
Abstract: An efficient, 8-step synthesis of (+)-α-cyperone (1) from (−)-α-santonin (5) is described. The key steps of the sequence involve the conversion of the keto ester 8 into the substituted octalone 9, by hydrogenation of the former in the presence of the homogeneous catalyst tris(triphenylphosphine)-chlororhodium, and the pyrolysis of the keto carbonate 16, which produces (+)-α-cyperone in good yield.