PFK-1 inhibitors, short for Phosphofructokinase-1 inhibitors, are a class of small molecules or compounds that play a pivotal role in the regulation of glycolysis, a fundamental metabolic pathway in living organisms. Glycolysis is the process by which glucose is broken down into pyruvate, generating adenosine triphosphate (ATP) molecules, which are essential for cellular energy production. PFK-1, or Phosphofructokinase-1, is a key enzyme within the glycolytic pathway, and it catalyzes the conversion of fructose-6-phosphate to fructose-1,6-bisphosphate. This step is considered the rate-limiting step of glycolysis, as it controls the flow of glucose through the pathway. PFK-1 inhibitors are compounds specifically designed to modulate the activity of this enzyme, thereby regulating the rate of glycolysis and affecting the overall metabolic state of the cell.
These inhibitors typically function by binding to PFK-1 and interfering with its enzymatic activity, thus slowing down the conversion of fructose-6-phosphate to fructose-1,6-bisphosphate. This leads to a reduction in the rate of glycolysis, ultimately impacting the cell's energy production and metabolic balance. PFK-1 inhibitors have garnered significant attention in both basic research and drug discovery efforts due to their potential to manipulate cellular metabolism. By altering glycolytic flux, these inhibitors can indirectly affect various cellular processes and pathways, making them valuable tools for studying cellular metabolism and its connections to various diseases.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
A glucose analog that competitively inhibits PFK-1 by replacing glucose in the glycolytic pathway, leading to decreased ATP production. | ||||||
Sodium dichloroacetate | 2156-56-1 | sc-203275 sc-203275A | 10 g 50 g | $54.00 $205.00 | 6 | |
Inhibits PFK-1 indirectly by increasing the activity of pyruvate dehydrogenase (PDH), diverting pyruvate away from glycolysis. | ||||||
Lonidamine | 50264-69-2 | sc-203115 sc-203115A | 5 mg 25 mg | $103.00 $357.00 | 7 | |
Disrupts PFK-1 activity by interfering with mitochondrial respiration and energy metabolism in cancer cells. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
A tyrosine kinase inhibitor that indirectly affects PFK-1 activity by inhibiting the signaling pathways necessary for glycolytic enzyme expression in certain cancer cells. | ||||||
Citric Acid Trisodium Salt | 68-04-2 | sc-214745 sc-214745A sc-214745B sc-214745C | 100 g 500 g 1 kg 5 kg | $40.00 $60.00 $80.00 $315.00 | ||
Inhibits PFK-1 allosterically by binding to the enzyme, thus limiting glycolytic flux. | ||||||
Gossypol | 303-45-7 | sc-200501 sc-200501A | 25 mg 100 mg | $114.00 $225.00 | 12 | |
A natural compound from cottonseed, inhibits PFK-1 by disrupting mitochondrial function and promoting apoptosis in cancer cells. | ||||||
Oxamic acid | 471-47-6 | sc-250620 | 25 g | $145.00 | ||
A competitive inhibitor of PFK-1 that competes with ATP for binding to the enzyme's active site. | ||||||