ECHDC3 inhibitors are a class of chemical compounds that specifically target and modulate the activity of the enzyme enoyl-CoA hydratase domain-containing 3 (ECHDC3). ECHDC3 is an enzyme that belongs to the hydratase/isomerase superfamily, playing a key role in the metabolism of fatty acids within the mitochondria. It is involved in the β-oxidation pathway, where it catalyzes the hydration of trans-2-enoyl-CoA derivatives, a crucial step in the breakdown of fatty acids to produce acetyl-CoA, which can then enter the citric acid cycle to generate energy. By influencing the activity of ECHDC3, these inhibitors can modulate the metabolic processes that govern the balance of lipid utilization and energy production within cells.
The mechanism by which ECHDC3 inhibitors function typically involves the binding of these compounds to the active site of the enzyme, where they can block the enzyme's ability to interact with its natural substrates. This inhibition can occur through competitive mechanisms, where the inhibitor competes with the substrate for the active site, or through non-competitive mechanisms, where the inhibitor binds to an alternative site on the enzyme, causing conformational changes that reduce its catalytic efficiency. By inhibiting ECHDC3, these compounds alter the flow of metabolites through the β-oxidation pathway, which can have downstream effects on cellular energy homeostasis, lipid storage, and overall metabolic regulation. ECHDC3 inhibitors are valuable tools in biochemical research, providing insights into the specific role of this enzyme in fatty acid metabolism and its broader implications in cellular energy dynamics. By studying these inhibitors, researchers can explore the complex interactions between lipid metabolism and other metabolic pathways, enhancing our understanding of how cells regulate energy production and manage metabolic stress.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(+)-Etomoxir sodium salt | 828934-41-4 | sc-215009 sc-215009A | 5 mg 25 mg | $151.00 $506.00 | 3 | |
Etomoxir inhibits CPT1, essential for the transport of fatty acids into mitochondria, thereby limiting the substrate availability for ECHDC3 in the beta-oxidation pathway. | ||||||
rac Perhexiline Maleate | 6724-53-4 | sc-460183 | 10 mg | $188.00 | ||
By inhibiting CPT enzymes, Perhexiline reduces fatty acid oxidation, potentially leading to lesser availability of substrates for ECHDC3 to act upon in the beta-oxidation process. | ||||||
Trimetazidine Dihydrochloride | 13171-25-0 | sc-220334 | 10 mg | $213.00 | ||
Acting on the beta-oxidation pathway, Trimetazidine inhibits enzymes such as 3-ketoacyl-CoA thiolase, which could reduce the activity of ECHDC3 by decreasing the downstream processing of fatty acids. | ||||||
Ranolazine | 95635-55-5 | sc-212769 | 1 g | $109.00 | 3 | |
Ranolazine partially inhibits beta-oxidation enzymes, which could result in a reduced function of ECHDC3 by decreasing the overall beta-oxidation activity in mitochondria. | ||||||
Meldonium | 76144-81-5 | sc-207887 | 100 mg | $455.00 | 1 | |
Meldonium's inhibition of gamma-butyrobetaine hydroxylase leads to decreased carnitine biosynthesis, thus diminishing fatty acid transport into mitochondria and indirectly reducing ECHDC3 activity in beta-oxidation. | ||||||
4-Hydroxy-L-phenylglycine | 32462-30-9 | sc-254680A sc-254680 | 5 g 10 g | $82.00 $109.00 | ||
By inhibiting carnitine acetyltransferase, Oxfenicine alters acyl-CoA levels and can indirectly suppress the activity of ECHDC3 in the beta-oxidation pathway by impacting substrate availability. | ||||||
α-Lipoic Acid | 1077-28-7 | sc-202032 sc-202032A sc-202032B sc-202032C sc-202032D | 5 g 10 g 250 g 500 g 1 kg | $69.00 $122.00 $212.00 $380.00 $716.00 | 3 | |
Alpha-lipoic acid's influence on mitochondrial function and the NADH/NAD+ ratio can indirectly affect the beta-oxidation process and subsequently reduce the functional activity of ECHDC3. | ||||||
Fenofibrate | 49562-28-9 | sc-204751 | 5 g | $41.00 | 9 | |
Although Fenofibrate typically upregulates beta-oxidation, it may paradoxically inhibit mitochondrial beta-oxidation, thereby potentially inhibiting ECHDC3's role in this metabolic pathway. | ||||||