Substituted pyranone inhibitors of cholesterol synthesis

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters

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560 60, 562470, 562469, 424308, 424310, C07C 6976

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active

044594224

ABSTRACT:
6-Phenyl-, phenylalkyl- and phenylethenyl-4-hydroxytetrahydropyran-2-ones in the 4(R)-trans stereoisomeric forms are potent inhibitors of cholesterol synthesis by virtue of their ability to inhibit the enzyme, 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

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Brown et al., J. Chem. Soc., Perkin I, (1976), 1165-1169.
Hulcher, Arch. Biochem & Biophys, 146, 422-427, (1971).
Singer et al., Proc. Soc. Exper. Biol. Med. 102, 370-373, (1959).
Meyer, Liebigs Ann. Chem., (1979), pp. 484-491.

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