New site-directed reversible inhibitors of 3-hydroxy-3-methylglutaryl-CoA reductase
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1992.tb16583.x/fullpdf
Reference25 articles.
1. 2. N. Qureshi, J. W. Porter, J. W. Porter, and S. L. Spurgeon (1981 ) inBiosynthesis of isoprenoid compounds () vol. 1 , p. 69 , Wiley, New York.
2. Competitive inhibition of 3-hydroxy-3-methylglutaryl coenzyme a reductase by ML-236A and ML-236B fungal metabolites, having hypocholesterolemic activity
3. Synthesis, SARs and therapeutic potential of HMG-CoA reductase inhibitors
4. New Substrates and Inhibitors of 3-Hydroxy-3-methylglutaryl-CoA Reductase
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1. Further Insights into the Mechanism of Action of Methylmalonyl-CoA Mutase by Electron Paramagnetic Resonance Studies;European Journal of Biochemistry;1997-10
2. Inactivation of 3-Hydroxy-3-methylglutaryl-CoA Synthase and Other Acyl-CoA-Utilizing Enzymes by 3-Oxobutylsulfoxyl-CoA;Biochemistry;1997-02-01
3. Inhibition of 3-Hydroxy-3-Methylglutaryl-CoA Reductase and Citrate Synthase by Sulfoxides and Sulfones of Substrate-analogue CoA-thioether Derivatives;European Journal of Biochemistry;1995-01
4. Chapter 23. New Potential Therapies for the Treatment of Atherosclerosis;Annual Reports in Medicinal Chemistry;1993
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