The group of chemical compounds known as Peroxin 1 Inhibitors primarily work through the modulation of lipid metabolism and peroxisome proliferation. HMG-CoA reductase inhibitors like Lovastatin, Atorvastatin, Pravastatin, Simvastatin, and Fluvastatin reduce cholesterol biosynthesis, a process that peroxisomes are involved in. The reduction in lipid biosynthesis can indirectly inhibit the functional activity of Peroxin 1 as it is involved in the biogenesis of peroxisomes. Therefore,the decreased demand for peroxisome biogenesis due to the lowered lipid biosynthesis could lead to the functional inhibition of Peroxin 1.
On the other hand, PPARα agonists such as Fenofibrate, Gemfibrozil, and Clofibrate, and PPARγ agonists like Rosiglitazone and Pioglitazone can increase the expression of genes involved in lipid metabolism, leading to an increase in peroxisome proliferation. This increased demand for peroxisomes could overwhelm the functional capacity of Peroxin 1, leading to its inhibition. Clotrimazole, which inhibits the biosynthesis of ergosterol, a process partially occurring in peroxisomes, can also lead to a decrease in Peroxin 1 activity. Similarly, Zileuton, a 5-lipoxygenase inhibitor, can decrease the production of leukotrienes metabolized in peroxisomes, leading to reduced Peroxin 1 activity due to decreased peroxisome need.
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