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pubmed-article:9871766pubmed:abstractTextMatrix metalloproteinase inhibitors of general formula (1) were synthesised by a route involving an Ireland-Claisen rearrangement which enables systematic modification of the substituent alpha to the hydroxamic acid. An analogue (12c) possessing an alpha-cyclopentyl group is a potent broad spectrum inhibitor that displays high and sustained blood levels following oral dosing in both the rat and marmoset ex-vivo bioassays. This compound and analogues are also potent inhibitors of TNF alpha release.lld:pubmed
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pubmed-article:9871766pubmed:articleTitleThe synthesis of novel matrix metalloproteinase inhibitors employing the Ireland-Claisen rearrangement.lld:pubmed
pubmed-article:9871766pubmed:affiliationBritish Biotech Pharmaceuticals Limited, Cowley, Oxford.lld:pubmed
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