Abstract
The studies described here, using enantiomers of an optically-active methoxy alkyl thiazole ICI216800 (1-methoxy-6-(naphth-2-yl-methoxy)-1-(thiazol-2-yl)indane), provide unequivocal evidence for a specific, chiral interaction with 5-lipoxygenase. In accordance with their biochemical efficacy these compounds also demonstrate enantio-specific anti-inflammatory activity in a leukotriene-mediated model of inflammation. This is the first class of compounds for which 5-lipoxygenase inhibition and anti-inflammatory activity have been shown to be mediated via a specific chiral interaction.
Cite
CITATION STYLE
McMillan, R. M., Girodeau, J. M., & Foster, S. J. (1990). Selective chiral inhibitors of 5-lipoxygenase with anti-inflammatory activity. British Journal of Pharmacology, 101(3), 501–503. https://doi.org/10.1111/j.1476-5381.1990.tb14111.x
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