Direct binding to sterols accelerates endoplasmic reticulum-associated degradation of HMG CoA reductase. [PDF]
Faulkner RA +4 more
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Antioxidant and Inhibitory Activities of Filipendula glaberrima Leaf Constituents against HMG-CoA Reductase and Macrophage Foam Cell Formation. [PDF]
Cho YB, Lee H, Jeon HJ, Lee JY, Kim HJ.
europepmc +1 more source
In vitro and in silico studies of the potential cytotoxic, antioxidant, and HMG CoA reductase inhibitory effects of chitin from Indonesia mangrove crab (Scylla serrata) shells. [PDF]
Fajriaty I +5 more
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In Silico Analysis of Selected Mikania Constituents As Human HMG-CoA Reductase, Human Inducible Nitric Oxide Synthase, and Human Squalene Synthase Inhibitory Agents. [PDF]
Vijayakumar STV +2 more
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Graft protective effects and donor-specific antibody suppression by CD4+CD25+Foxp3+ regulatory T cell induced by HMG-CoA reductase inhibitor rosuvastatin in a murine heart transplant model. [PDF]
Iguchi K +7 more
europepmc +1 more source
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Since in humans the greater part of the cholesterol in the body is synthesized de novo in the liver and intestine, the search for drugs to inhibit cholesterol biosynthesis has long been pursued as a means to lower the level of plasma cholesterol and so help to prevent and treat atherosclerosis.
A, Endo, K, Hasumi
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Beta-hydroxy-beta-methylglutaryl coenzyme A (HMG CoA) reductase inhibitors (HMG CoA RIs) are now being prescribed in many different countries, and the number of patients treated with these compounds is estimated to be over 1.5 million. The spectrum of indications for these drugs is enlarging.
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HMG CoA (β-hydroxy-β-methylglutaryl coenzyme A) reductase inhibitors are very effective in lowering total and low-density lipoprotein cholesterol. The incidence of adverse effects is very low with elevated transaminase levels and myopathy being of greatest concern.
M J Ashton, G Fenton
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