CARKD inhibitors are a class of chemical compounds that specifically target and inhibit the activity of CARKD, or CAR kinase domain-containing protein. CARKD is involved in cellular energy metabolism, particularly in the regulation of key metabolic pathways. It is associated with the phosphorylation of proteins that participate in metabolic control, including enzymes involved in the management of cellular energy stores such as ATP and NAD+. By inhibiting CARKD, these compounds interfere with its kinase activity, disrupting its ability to phosphorylate substrate proteins and thereby affecting the overall regulation of metabolic processes. This can lead to alterations in energy balance within the cell, impacting functions like biosynthesis, energy production, and catabolism.
The structure and action of CARKD inhibitors can vary, but they typically work by binding to the active site of the kinase domain, preventing CARKD from interacting with its target proteins or transferring phosphate groups. Some inhibitors may also modify the protein's conformation, blocking its ability to function in a normal enzymatic manner. Researchers utilize CARKD inhibitors to study the broader implications of metabolic regulation and how CARKD influences cellular energy homeostasis. Inhibiting CARKD provides valuable insights into the role of protein phosphorylation in metabolic pathways, particularly in processes like glycolysis, oxidative phosphorylation, and fatty acid metabolism. These inhibitors are crucial for understanding how energy regulation is coordinated at the molecular level and for exploring the network of signaling pathways that maintain cellular metabolic balance.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | ¥824.00 ¥2685.00 ¥8089.00 ¥28453.00 ¥241660.00 | 53 | |
与 DNA 相互结合,抑制 RNA 聚合酶,影响基因和假基因的转录。 | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | ¥2933.00 ¥11609.00 | 26 | |
抑制 RNA 聚合酶 II,这可能会减少由该聚合酶转录的假基因的转录。 | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | ¥1072.00 ¥3633.00 ¥7480.00 ¥16224.00 | 6 | |
与细菌 RNA 聚合酶结合,但在高浓度下也可能影响真核生物 RNA 聚合酶。 | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | ¥993.00 ¥2256.00 | 13 | |
一种二萜三环氧化物,可抑制 RNA 聚合酶 I、II 和 III 的转录活性。 | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | ¥1117.00 | 5 | |
由于其结构与腺苷相似,但缺少羟基,因此可终止 RNA 链的伸长。 | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | ¥474.00 ¥2087.00 ¥3497.00 ¥7333.00 | 6 | |
抑制 RNA 聚合酶 II 的转录延伸。 | ||||||
Leptomycin B | 87081-35-4 | sc-358688 sc-358688A sc-358688B | 50 µg 500 µg 2.5 mg | ¥1185.00 ¥4603.00 ¥13809.00 | 35 | |
抑制 RNA 分子从细胞核中输出,从而可能影响假基因 RNA 的加工。 | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | ¥124.00 ¥192.00 ¥1218.00 ¥2764.00 ¥10357.00 ¥553.00 | 33 | |
一种具有抗炎和抗氧化特性的类黄酮,可调节基因表达和 RNA 稳定性。 | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | ¥1038.00 ¥2933.00 | 42 | |
一种可影响转录调节的细胞周期蛋白依赖性激酶抑制因子。 | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | ¥2550.00 ¥9545.00 | 1 | |
Bromodomain 抑制剂,可破坏乙酰化组蛋白的结合,从而可能改变染色质结构和基因表达。 |