Muscle fructose-1,6-bisphosphatase (FBPase) inhibitors constitute a class of compounds that modulate the activity of muscle FBPase, an enzyme primarily involved in gluconeogenesis, the metabolic pathway responsible for the generation of glucose from non-carbohydrate sources. Muscle FBPase plays a critical role in regulating glucose levels by catalyzing the hydrolysis of fructose-1,6-bisphosphate into fructose-6-phosphate and inorganic phosphate, which is one of the last steps in the gluconeogenesis pathway. Inhibition of muscle FBPase affects the balance between glucose production and utilization within the body.
The action of muscle FBPase inhibitors can be direct, where the inhibitor molecules bind to the active site or allosteric sites of the enzyme, thereby reducing its catalytic activity. These inhibitors often mimic the structure of the enzyme's natural substrates or products, competitively blocking access to the active site, or they may induce conformational changes that reduce the enzyme's affinity for its substrates. Indirect inhibition may occur through modulation of signaling pathways that regulate the enzyme's activity or expression. For example, certain inhibitors may interfere with the transcriptional control mechanisms of the FBPase gene or modify post-translational modifications that affect the enzyme's stability or activity. Research into muscle FBPase inhibitors is driven by the desire to understand the regulation of glucose metabolism in various physiological and pathophysiological states. Through the study of these inhibitors, scientists aim to elucidate the intricate control mechanisms governing energy homeostasis and the response of metabolic pathways to various intracellular and extracellular signals.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Adenosine phosphate(Vitamin B8) | 61-19-8 | sc-278678 sc-278678A | 50 g 100 g | $160.00 $240.00 | ||
AMP is an endogenous inhibitor of FBPase. Elevated AMP levels signal energy depletion in muscle cells and inhibit FBPase, slowing gluconeogenesis. | ||||||
C75 (racemic) | 191282-48-1 | sc-202511 sc-202511A sc-202511B | 1 mg 5 mg 10 mg | $71.00 $202.00 $284.00 | 9 | |
C75 is a synthetic compound that indirectly inhibits FBPase by modulating fatty acid metabolism and reducing malonyl-CoA levels, which leads to AMPK activation. | ||||||
A-769662 | 844499-71-4 | sc-203790 sc-203790A sc-203790B sc-203790C sc-203790D | 10 mg 50 mg 100 mg 500 mg 1 g | $180.00 $726.00 $1055.00 $3350.00 $5200.00 | 23 | |
A769662 is a small molecule that directly activates AMPK, resulting in FBPase inhibition and decreased gluconeogenesis. | ||||||
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
2-Deoxyglucose is a glucose analogue that competitively inhibits FBPase, interfering with gluconeogenesis by reducing the availability of fructose-1,6-bisphosphate. | ||||||
Phosphoenolpyruvic acid, monopotassium salt | 4265-07-0 | sc-208168 sc-208168A sc-208168B | 100 mg 250 mg 1 g | $76.00 $152.00 $296.00 | 1 | |
PEP is a substrate analogue that can competitively inhibit FBPase by binding to its active site, preventing the hydrolysis of fructose-1,6-bisphosphate. | ||||||
Berberine | 2086-83-1 | sc-507337 | 250 mg | $90.00 | 1 | |
Berberine is a natural compound that activates AMPK, leading to FBPase inhibition and reduced gluconeogenesis. | ||||||
Rosiglitazone | 122320-73-4 | sc-202795 sc-202795A sc-202795C sc-202795D sc-202795B | 25 mg 100 mg 500 mg 1 g 5 g | $118.00 $320.00 $622.00 $928.00 $1234.00 | 38 | |
While primarily used as a PPARγ agonist for diabetes, rosiglitazone can indirectly inhibit FBPase by improving insulin sensitivity and reducing gluconeogenesis in muscle tissue. | ||||||