Date published: 2025-9-13

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FADS6 Activators

Pioglitazone and Rosiglitazone, elevate gene transcription for fatty acid metabolism, thereby potentially boosting FADS6 expression and activity. Fenofibrate, a PPAR alpha agonist, might similarly augment FADS6 activity by enhancing fatty acid catabolism and substrate availability. AMPK activators such as AICAR and 1,1-Dimethylbiguanide, Hydrochloride are integral to this class, shifting cellular energy balance towards fatty acid oxidation, which in turn could upregulate FADS6 activity. Nutrient-derived polyphenols and flavonoids, like Resveratrol and Quercetin, contribute to this class by influencing lipid metabolism and altering gene expression, which can indirectly affect the enzymatic function of FADS6. Additionally, fatty acid components such as EPA and DHA modify fatty acid composition within cellular membranes, potentially leading to a dynamic adjustment in FADS6 activity.

SRT1720, as a SIRT1 activator, impacts epigenetic regulation of metabolism-related genes, which could result in altered FADS6 activity. Berberine stands out for its role in lipid metabolism modulation, suggesting a possible influence on FADS6 through various metabolic pathways. Each compound in this class does not interact directly with FADS6 but instead exerts an effect on the enzyme's activity by modulating different cellular processes, such as gene expression, fatty acid metabolism, cellular energy states, and epigenetic landscapes.

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