Aldehyde Dehydrogenase Activators encompass a range of compounds that indirectly or directly enhance the enzyme's activity, playing a crucial role in metabolizing various aldehydes and contributing to cellular detoxification processes. Disulfiram, Cyanamide, Calcium carbimide, and Coprine function as inhibitors of Aldehyde Dehydrogenase, but paradoxically, they enhance its functional demand by causing an accumulation of acetaldehyde, a primary substrate for the enzyme. This accumulation necessitates increased activity of Aldehyde Dehydrogenase to metabolize the excess acetaldehyde, thus indirectly boosting its functional role. Similarly, Daidzin, as an isoflavone inhibitor, increases the requirement for Aldehyde Dehydrogenase in aldehyde metabolism. Fomepizole, although primarily an alcohol dehydrogenase inhibitor, influences Aldehyde Dehydrogenase activity by altering alcohol metabolism, thereby indirectly enhancing the enzyme's role in acetaldehyde metabolism.
On the other hand, compounds like Chloral hydrate, Citral, Benzaldehyde, Acetaldehyde, Retinal, and Malondialdehyde serve as direct substrates for Aldehyde Dehydrogenase, actively engaging and increasing the enzyme's metabolic activity. The metabolism of Chloral hydrate into trichloroacetic acid, Citral into various metabolites, Benzaldehyde into benzoic acid, and Malondialdehyde into less toxic compounds, each involves the direct participation of Aldehyde Dehydrogenase, showcasing its critical role in metabolizing these diverse compounds. The conversion of Retinal to retinoic acid is another key process facilitated by Aldehyde Dehydrogenase, highlighting its importance in vision and cellular differentiation. Collectively, these activators, through their direct and indirect interactions with Aldehyde Dehydrogenase, underscore the enzyme's essential function in various physiological processes, including detoxification, metabolism, and cellular signaling.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Disulfiram inhibits Aldehyde Dehydrogenase by binding to its copper cofactor, resulting in the accumulation of acetaldehyde. This inhibition indirectly enhances the detoxification role of Aldehyde Dehydrogenase by increasing its demand and activity in cells. | ||||||
Cyanamide | 420-04-2 | sc-239592 sc-239592A | 5 g 25 g | $21.00 $77.00 | ||
Cyanamide acts as an allosteric inhibitor of Aldehyde Dehydrogenase. By inhibiting the enzyme, it increases the need for Aldehyde Dehydrogenase activity in detoxification pathways, thereby enhancing its overall functional role in the body. | ||||||
Fomepizole | 7554-65-6 | sc-252838 | 1 g | $74.00 | 1 | |
Fomepizole, primarily an inhibitor of alcohol dehydrogenase, can also influence Aldehyde Dehydrogenase activity. By altering the alcohol metabolism pathway, Fomepizole indirectly enhances the role of Aldehyde Dehydrogenase in metabolizing acetaldehyde. | ||||||
Daidzin | 552-66-9 | sc-202123 sc-202123A | 1 mg 5 mg | $71.00 $134.00 | 1 | |
Daidzin is an isoflavone that acts as an inhibitor of Aldehyde Dehydrogenase. By inhibiting the enzyme, Daidzin indirectly increases the demand for Aldehyde Dehydrogenase activity in pathways involved in aldehyde metabolism. | ||||||
Trichloroacetaldehyde-13C2 | sc-474862 | 2.5 mg | $380.00 | |||
Chloral hydrate is metabolized by Aldehyde Dehydrogenase into trichloroacetic acid. This process directly engages Aldehyde Dehydrogenase, enhancing its activity as part of the metabolism of chloral hydrate. | ||||||
Citral | 5392-40-5 | sc-252620 | 1 kg | $212.00 | ||
Citral is metabolized by Aldehyde Dehydrogenase, leading to an increase in enzyme activity. This metabolism process directly involves Aldehyde Dehydrogenase, enhancing its functional role in breaking down citral. | ||||||