Substituted cyclohexene derivatives as HMG-CoA reductase inhibit

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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549292, 558270, 558271, 558272, 560 9, 560 12, 560 13, 560 14, 560 27, 560 39, 560 31, 560 32, 562429, 562430, 562431, 562441, 562469, 546268, 546296, 546297, 546298, 546301, 546302, 546300, 546307, 546309, 546153, 546155, 546159, 546162, 514478, 514512, 514532, 514533, 514542, 514559, 514570, 514562, 514563, 514459, 514460, 514414, 514418, 514824, 514313, 514336, 514352, 514318, 514341, 514351, 514315, 548467, 548472, 548475, A61K 3117, A61K 31365, C07D21516, C07D30910

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051323125

ABSTRACT:
Disclosed are novel 3-hydroxy-3-methylglutarylcoenzyme A reductase inhibitors useful as antihypercholesterolemic agents represented by the formula ##STR1## and the corresponding ring-opened hydroxy acids derived therefrom and pharmaceutically acceptable salts thereof.
Pharmaceutical compositions containing said compounds and method of inhibiting the biosynthesis of cholesterol therewith are also disclosed.

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patent: 4611067 (1986-09-01), Volante et al.
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patent: 4668699 (1987-05-01), Hoffman et al.
patent: 4681893 (1987-07-01), Roth
patent: 4772629 (1988-09-01), Smith et al.

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