CYP4F11 inhibitors are a class of chemical compounds that specifically target and modulate the activity of the cytochrome P450 4F11 enzyme, which is a member of the cytochrome P450 (CYP) superfamily of enzymes. Cytochrome P450 enzymes are critical for the metabolism of a wide range of endogenous and exogenous compounds in the human body, including drugs, toxins, and various endogenous molecules. CYP4F11, in particular, plays a significant role in the oxidation of fatty acids and eicosanoid metabolism. These enzymes are primarily found in the liver and various extrahepatic tissues, where they participate in the detoxification and elimination of xenobiotics, as well as the regulation of lipid homeostasis. CYP4F11 inhibitors are designed to selectively inhibit the activity of this specific enzyme, which can have important implications for understanding its physiological roles and potential applications in various research areas.
Researchers have been interested in CYP4F11 inhibitors for their potential to elucidate the enzyme's involvement in fatty acid metabolism and eicosanoid biosynthesis. By inhibiting CYP4F11, scientists can gain insights into the specific functions of this enzyme and its impact on lipid signaling pathways. Additionally, CYP4F11 inhibitors can serve as valuable tools in studies related to the role of eicosanoids in various physiological and pathological processes, as well as their potential links to inflammation, cardiovascular diseases, and cancer. These inhibitors can also aid in deciphering the complex interplay between different cytochrome P450 enzymes and their contributions to the overall metabolism of lipids and other bioactive compounds within the body.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Montelukast Sodium | 151767-02-1 | sc-202231 sc-202231A sc-202231B | 10 mg 25 mg 250 mg | $51.00 $85.00 $161.00 | 5 | |
Montelukast, a leukotriene receptor antagonist, indirectly inhibits CYP4F11 by modulating leukotriene pathways, which CYP4F11 is involved in metabolizing. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin is a flavonoid that inhibits CYP4F11 by binding to its active site, thus interfering with its metabolic activity. | ||||||
Ketoconazole | 65277-42-1 | sc-200496 sc-200496A | 50 mg 500 mg | $63.00 $265.00 | 21 | |
Ketoconazole also inhibits CYP4F11 by interacting with the heme group of the cytochrome P450 enzymes. | ||||||
Miconazole | 22916-47-8 | sc-204806 sc-204806A | 1 g 5 g | $66.00 $160.00 | 2 | |
Similar to Ketoconazole, Miconazole inhibits CYP4F11 through its interaction with the enzyme's heme group. | ||||||
Clotrimazole | 23593-75-1 | sc-3583 sc-3583A | 100 mg 1 g | $42.00 $57.00 | 6 | |
Clotrimazole inhibits CYP4F11 by binding to its active site, affecting the enzyme's metabolic functions. | ||||||
Fluconazole | 86386-73-4 | sc-205698 sc-205698A | 500 mg 1 g | $54.00 $84.00 | 14 | |
Fluconazole is known to inhibit CYP4F11, reducing its ability to metabolize substrates through competitive inhibition. | ||||||
(±)-Sulfinpyrazone | 57-96-5 | sc-202822 sc-202822A | 1 g 5 g | $42.00 $94.00 | 2 | |
Sulfinpyrazone inhibits CYP4F11 by competitively binding to its active site, thus impacting its role in drug metabolism. | ||||||
Fluoxetine | 54910-89-3 | sc-279166 | 500 mg | $318.00 | 9 | |
Fluoxetine inhibits CYP4F11 through competitive binding to the enzyme's active site, affecting its metabolic functions. | ||||||
Paroxetine | 61869-08-7 | sc-507527 | 1 g | $180.00 | ||
Paroxetine inhibits CYP4F11 by binding to its active site, altering the enzyme's ability to process its substrates. | ||||||