Selective chiral inhibitors of 5‐lipoxygenase with anti‐inflammatory activity

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 c...

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Veröffentlicht in:British journal of pharmacology 1990-11, Vol.101 (3), p.501-503
Hauptverfasser: McMillan, R.M., Girodeau, J.‐M., Foster, S.J.
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:0007-1188
1476-5381
DOI:10.1111/j.1476-5381.1990.tb14111.x