Equally potent inhibitors of cholesterol synthesis in human hepatocytes have distinguishable effects on different cytochrome P450 enzymes-Reference-Cited by-同舟云学术

Equally potent inhibitors of cholesterol synthesis in human hepatocytes have distinguishable effects on different cytochrome P450 enzymes

Published:2000-12 Issue:9 Volume:21 Page:353-364
ISSN:0142-2782
Container-title:Biopharmaceutics & Drug Disposition
language:en
Short-container-title:Biopharm. Drug Dispos.

Author:

Cohen L.H.,van Leeuwen R.E.W.,van Thiel G.C.F.,van Pelt J.F.,Yap S.H.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine

Reference43 articles.

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3. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 4. Side-chain ester derivatives of mevinolin

4. Hypolipoproteinemic activity of XU 62-320, a potent competitive inhibitor of HMG-CoA reductase. In Eighth International Symposium on Atherosclerosis, Rome. CIC Edizioni Internazionali: Rome. 1988; 230.

5. Hepatic and nonhepatic sterol synthesis and tissue distribution following administration of a liver selective HMG-CoA reductase inhibitor, CI-981: Comparison with selected HMG-CoA reductase inhibitors

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