SNX17 Inhibitors are a class of chemical compounds designed to target and inhibit the function of Sorting Nexin 17 (SNX17), a member of the sorting nexin family involved in endosomal trafficking and receptor recycling. SNX17 plays a crucial role in mediating the endocytosis and subsequent recycling of various cell surface receptors, including integrins and low-density lipoprotein receptors, back to the plasma membrane. By binding to these receptors, SNX17 helps maintain their proper localization and function within the cell. The inhibition of SNX17 disrupts this process, leading to alterations in receptor trafficking, which can impact various cellular functions, including cell adhesion, migration, and signal transduction.
The study of SNX17 Inhibitors provides valuable insights into the mechanisms of receptor trafficking and the broader implications of endosomal sorting on cellular homeostasis. By selectively inhibiting SNX17, researchers can dissect the pathways that depend on proper receptor recycling and explore how disruptions in these pathways affect cellular behavior. This is particularly relevant in understanding how cells regulate their surface receptor composition in response to environmental cues or during processes like cell migration and immune responses. Additionally, SNX17 Inhibitors offer a tool to investigate the interactions between SNX17 and other proteins involved in endosomal sorting, revealing the complex network of interactions that govern intracellular trafficking. Overall, SNX17 Inhibitors serve as a crucial resource for studying the dynamic processes of endocytosis and receptor recycling, contributing to a deeper understanding of cellular regulation and the maintenance of cellular function.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
BMH-21 | 896705-16-1 | sc-507460 | 10 mg | ¥1862.00 | ||
这种化合物还抑制动力蛋白,因此可以破坏内吞作用,可能影响PSGL1进入内吞体的循环。 | ||||||
MRT67307 | 1190378-57-4 | sc-507433 | 10 mg | ¥2640.00 | ||
MRT67307抑制TBK1和IKKε,它们在内吞体运输中发挥作用,特别是与自噬体形成有关。 | ||||||
Latrunculin A, Latrunculia magnifica | 76343-93-6 | sc-202691 sc-202691B | 100 µg 500 µg | ¥2933.00 ¥9014.00 | 36 | |
通过结合肌动蛋白,拉曲秦A可破坏肌动蛋白聚合。肌动蛋白细胞骨架对于许多内吞过程至关重要。 | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | ¥654.00 ¥936.00 ¥1579.00 ¥2730.00 | 38 | |
该化合物可破坏微管聚合。微管对于囊泡运输和内吞体运输至关重要。 | ||||||
Chlorpromazine | 50-53-3 | sc-357313 sc-357313A | 5 g 25 g | ¥677.00 ¥1218.00 | 21 | |
氯丙嗪可抑制由衣藻素介导的内吞作用,从而可能影响内吞体的运输路径。 | ||||||
5-(N-Ethyl-N-isopropyl)-Amiloride | 1154-25-2 | sc-202458 | 5 mg | ¥1151.00 | 20 | |
5-(N-乙基-N-异丙基)阿米洛利是一种巨噬细胞吞噬作用的强效抑制剂,该作用与内吞作用和内体运输密切相关。 | ||||||
Monensin A | 17090-79-8 | sc-362032 sc-362032A | 5 mg 25 mg | ¥1715.00 ¥5810.00 | ||
莫能菌素是一种离子载体,可破坏内体-溶酶体运输。由于蛋白质分拣受到干扰,这可能会影响SNX33的表达。 | ||||||
Autophagy Inhibitor, 3-MA | 5142-23-4 | sc-205596 sc-205596A | 50 mg 500 mg | ¥632.00 ¥2888.00 | 113 | |
3-MA抑制PI3K,已知会影响自噬。鉴于内体和自噬体之间的关系,SNX33的表达可能会受到影响。 | ||||||
Niclosamide | 50-65-7 | sc-250564 sc-250564A sc-250564B sc-250564C sc-250564D sc-250564E | 100 mg 1 g 10 g 100 g 1 kg 5 kg | ¥417.00 ¥869.00 ¥2076.00 ¥5754.00 ¥13809.00 ¥65594.00 | 8 | |
尼氯沙胺通过干扰SNX8在Wnt信号传导中的作用来抑制其活性,导致内体货物分拣中断。 |