ALDH1A3 inhibitors belong to a class of chemical compounds designed to target and inhibit the enzyme aldehyde dehydrogenase 1A3 (ALDH1A3). This enzyme is a member of the ALDH superfamily and plays a crucial role in the oxidation of aldehydes to their corresponding carboxylic acids, a vital metabolic process in cells. ALDH1A3, specifically, is implicated in the oxidation of retinaldehyde to retinoic acid, a biologically active form of vitamin A. This enzymatic activity is essential for various cellular processes, including the regulation of gene expression, cell differentiation, and tissue development. Consequently, the inhibition of ALDH1A3 can have significant biochemical consequences.
The design and development of ALDH1A3 inhibitors are primarily driven by their potential applications in research and drug discovery. Researchers utilize these inhibitors to investigate the biological functions of ALDH1A3, especially in the context of cellular differentiation and retinoic acid signaling pathways. Additionally, ALDH1A3 inhibitors can be valuable tools for understanding the role of this enzyme in various diseases, such as cancer, where aberrant retinoic acid signaling has been implicated. By selectively inhibiting ALDH1A3, researchers can gain insights into the molecular mechanisms underlying these diseases
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tolcapone | 134308-13-7 | sc-220266 | 10 mg | $167.00 | 1 | |
Tolcapone has also been investigated for its ALDH1A3 inhibitory activity in cancer models. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Disulfiram, an approved drug for alcohol dependence, has shown ALDH1A3 inhibitory activity and is being repurposed for cancer research. |