Hexokinase inhibitors are a class of chemical compounds designed to specifically target and inhibit the activity of hexokinase, a key enzyme in the glycolytic pathway. Hexokinase catalyzes the first step in glycolysis by phosphorylating glucose to glucose-6-phosphate, a crucial process for glucose metabolism in cells. Inhibiting hexokinase activity disrupts this fundamental step, effectively reducing the rate of glycolysis and subsequent production of energy in the form of ATP. Hexokinase is also known to associate with mitochondria, and its inhibition can interfere with the enzyme's role in regulating metabolic pathways, apoptosis, and mitochondrial function. The ability of hexokinase inhibitors to block this enzyme makes them valuable tools for investigating cellular metabolism and energy production in various biological systems.
In research, hexokinase inhibitors are employed to explore the metabolic adaptations and consequences of glycolytic inhibition in cells. These inhibitors are particularly useful in studying the metabolic flexibility of cells, especially in understanding how they respond to changes in glucose availability or glycolytic flux. By blocking hexokinase activity, researchers can examine shifts in alternative metabolic pathways, such as oxidative phosphorylation or fatty acid oxidation, providing insights into cellular energy homeostasis and adaptability. Additionally, hexokinase inhibitors can shed light on the regulation of glucose metabolism in different tissues and organisms, facilitating studies on the role of metabolic enzymes in maintaining cellular function under various physiological and environmental conditions. These inhibitors offer a powerful approach to probing the complex interactions between metabolism, cellular signaling, and energy regulation.
関連項目
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
这种葡萄糖类似物会被己糖激酶磷酸化,但不能进行进一步的新陈代谢,因此会与葡萄糖竞争,抑制其转化为葡萄糖-6-磷酸。 | ||||||
N-Acetyl-D-glucosamine | 7512-17-6 | sc-286377 sc-286377B sc-286377A | 50 g 100 g 250 g | $92.00 $159.00 $300.00 | 1 | |
作为一种竞争性抑制剂,它与酶的活性位点结合,阻止葡萄糖被磷酸化。 | ||||||
Lonidamine | 50264-69-2 | sc-203115 sc-203115A | 5 mg 25 mg | $103.00 $357.00 | 7 | |
能与己糖激酶 II 特异性结合,破坏其与线粒体电压依赖性阴离子通道的相互作用,抑制其酶活性。 | ||||||
D-(−)-Fructose | 57-48-7 | sc-221456 sc-221456A sc-221456B | 100 g 500 g 5 kg | $40.00 $89.00 $163.00 | 3 | |
可作为己糖激酶的底物,但亲和力远低于葡萄糖;大量存在时可与葡萄糖竞争。 | ||||||
D-Glucosamine | 3416-24-8 | sc-278917A sc-278917 | 1 g 10 g | $197.00 $764.00 | ||
作为一种竞争性抑制剂,它与酶的活性位点结合,阻止葡萄糖发生磷酸化。 | ||||||
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 | |
虽然它主要是一种抗糖尿病药物,但它可以通过对细胞葡萄糖摄取和利用的影响间接调节己糖激酶的活性。 |