Abstract
A series of disubstituted thiazoles, functionalized with the essential 3,5-dihydroxy-6-heptenoic or heptanoic chain, were prepared and evaluated for their ability to inhibit the enzyme HMG-CoA reductase in vitro. All the synthesized compounds 46-61 showed a moderate inhibitory potency.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Hydroxymethylglutaryl-CoA Reductase Inhibitors*
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In Vitro Techniques
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Liver / enzymology
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Molecular Structure
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Rats
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Structure-Activity Relationship
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Thiazoles / chemical synthesis
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Thiazoles / chemistry
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Thiazoles / pharmacology*
Substances
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Hydroxymethylglutaryl-CoA Reductase Inhibitors
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Thiazoles