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Thiazole analogues of the NSAID indomethacin as selective COX-2 inhibitors
K W Woods1, R W McCroskey, M R Michaelides
1Abbott Laboratories, Abbott Park, IL 60064-6101, USA. keith.woods@abbott.com
Abstract:
The carboxyl group of the NSAID indomethacin was replaced with a variety of substituted thiazoles to obtain a series of potent, selective inhibitors of COX-2. Additional substitutions were made at the 1-position and 5-position of the indole of indomethacin.
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