ALDH4A1 inhibitors belong to a specific chemical class of compounds designed to target and inhibit the activity of the enzyme aldehyde dehydrogenase 4 family member A1 (ALDH4A1). This enzyme is responsible for catalyzing the conversion of succinic semialdehyde to succinate during the lysine degradation pathway. By inhibiting ALDH4A1, these compounds disrupt the enzymatic reaction, thereby preventing the conversion of succinic semialdehyde. As a consequence, the accumulation of succinic semialdehyde occurs, leading to alterations in biochemical pathways associated with lysine metabolism. ALDH4A1 inhibitors are designed based on their interactions with the active site of the ALDH4A1 enzyme, typically through reversible or irreversible binding. The chemical structures of these inhibitors are strategically tailored to fit within the enzyme's active site, thereby disrupting its catalytic function.
By inhibiting ALDH4A1, these compounds have the potential to affect cellular metabolism and signaling pathways that involve lysine degradation, which may have important implications in various biological processes. Researchers and scientists study ALDH4A1 inhibitors to better understand the intricacies of lysine metabolism and the role of ALDH4A1 in cellular homeostasis. This class of inhibitors also provides a valuable tool for investigating the biochemical consequences of inhibiting ALDH4A1, shedding light on potential cellular responses and regulatory mechanisms related to lysine degradation. The development and study of ALDH4A1 inhibitors have opened up new avenues of research in biochemistry, cellular biology, and pharmacology, helping to advance our understanding of enzyme inhibition and its impact on metabolic pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Salicylhydroxamic acid | 89-73-6 | sc-236849 | 5 g | $20.00 | ||
SHAM is a derivative of salicylic acid and has been studied as an inhibitor of ALDH4A1. | ||||||
5-Methoxytryptamine | 608-07-1 | sc-325556 sc-325556A | 1 g 5 g | $80.00 $238.00 | ||
Also known as melatonin, this compound has been studied for its inhibitory effects on ALDH4A1. | ||||||
Catechin | 154-23-4 | sc-205624 sc-205624A | 1 mg 5 mg | $133.00 $299.00 | 3 | |
Catechin is a natural flavonoid that has been investigated for its potential inhibitory activity against ALDH4A1. | ||||||
Theophylline | 58-55-9 | sc-202835 sc-202835A sc-202835B | 5 g 25 g 100 g | $20.00 $32.00 $85.00 | 6 | |
Theophylline is a xanthine derivative and has been reported to inhibit ALDH4A1 in certain studies. | ||||||