Date published: 2026-2-22

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CYP4A31 Activators

CYP4A31 is a gene belonging to the cytochrome P450 superfamily, specifically within the CYP4 family that includes various subfamilies from CYP4A to CYP4M. The proteins encoded by this family, including CYP4A31, are primarily involved in the oxidation of organic substances. CYP4A31, like its counterparts, plays a significant role in metabolizing fatty acids, particularly through the hydroxylation of the terminal omega-carbon of both saturated and unsaturated fatty acids. This enzymatic activity is crucial for processing fatty acids into forms that can be further utilized or broken down within biological systems.

The expression of CYP4A31 can be induced by certain chemical compounds. For instance, 5-Aminoimidazole-4-carboxyamide-ribonucleoside (AICAR), a known activator of AMP-activated protein kinase (AMPK), has been observed to increase the expression of CYP4A31. This induction is mediated through the peroxisome proliferator-activated receptor α (PPARα), a nuclear receptor that plays a pivotal role in the regulation of gene expression involved in lipid metabolism. Although the complete physiological and metabolic functions of CYP4A31 are not entirely elucidated, the interest in this enzyme has grown due to its role in cell signaling processes and alternative pathways for fatty acid metabolism. The ability of CYP4A31 and other CYP4A enzymes to hydroxylate fatty acids may have significant implications for various biological processes, including the regulation of blood flow in specific organs and tissues.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

AICAR

2627-69-2sc-200659
sc-200659A
sc-200659B
50 mg
250 mg
1 g
$65.00
$280.00
$400.00
48
(2)

AICAR, a prodrug activator of AMPK, has been shown to increase the hepatic expression of CYP4A31 mRNA. Its effect is mediated through a PPARα-dependent mechanism, as it does not elicit changes in PPARα null mice. AICAR's induction of CYP4A31 expression suggests its involvement in activating pathways linked to PPARα.