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
製品名 | CAS # | カタログ # | 数量 | 価格 | 引用文献 | レーティング |
---|---|---|---|---|---|---|
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
このグルコース類似体はヘキソキナーゼによってリン酸化されるが、それ以上の代謝を受けることができないため、グルコースと競合し、グルコース-6-リン酸への変換を阻害する。 | ||||||
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 | |
酵素の活性部位に結合することで競合阻害剤として働き、グルコースがリン酸化されるのを防ぐ。 | ||||||
Lonidamine | 50264-69-2 | sc-203115 sc-203115A | 5 mg 25 mg | $103.00 $357.00 | 7 | |
ヘキソキナーゼIIに特異的に結合し、ミトコンドリアの電位依存性アニオンチャネルとの相互作用を阻害し、その酵素活性を阻害する。 | ||||||
D-(−)-Fructose | 57-48-7 | sc-221456 sc-221456A sc-221456B | 100 g 500 g 5 kg | $40.00 $89.00 $163.00 | 3 | |
ヘキソキナーゼの基質となるが、親和性はグルコースよりはるかに低く、多量に存在するとグルコースと競合する。 | ||||||
D-Glucosamine | 3416-24-8 | sc-278917A sc-278917 | 1 g 10 g | $197.00 $764.00 | ||
酵素の活性部位に結合し、グルコースがリン酸化されるのを阻害する。 | ||||||
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 | |
主に抗糖尿病薬であるが、ヘキソキナーゼ活性は、細胞のグルコース取り込みと利用に対する作用を通して間接的に調節することができる。 |