Rab 24 inhibitors are a class of chemical compounds that specifically target the Rab24 protein, a member of the Rab GTPase family. Rab proteins, including Rab24, are small GTP-binding proteins that play a crucial role in vesicular trafficking, which is the process of moving vesicles within cells. Rab24, in particular, is involved in the regulation of autophagy, a cellular degradation process that clears damaged proteins and organelles, and its function is linked to various cellular processes such as lysosomal degradation and cellular response to stress. The inhibition of Rab24 can disrupt these processes, providing a means to study the mechanistic pathways involved in vesicular trafficking and autophagy. Rab24 inhibitors are therefore valuable tools in molecular and cell biology research for dissecting the specific roles of Rab24 in cellular homeostasis and the broader network of Rab GTPases.
The development and characterization of Rab24 inhibitors involve a combination of chemical biology, structural biology, and high-throughput screening techniques. These inhibitors are typically small molecules designed to bind to the GTP-binding domain of Rab24, preventing its interaction with downstream effectors and thus inhibiting its activity. Structural studies, including X-ray crystallography and NMR spectroscopy, are often employed to determine the precise binding modes of these inhibitors, enabling further optimization of their specificity and potency. Additionally, understanding the off-target effects of Rab24 inhibitors is crucial for accurately interpreting experimental results, as these compounds may interact with other proteins or cellular components. By selectively modulating Rab24 activity, researchers can explore its unique contribution to cellular dynamics and autophagy, offering insights into the fundamental mechanisms that govern cell physiology and pathology. These insights are critical for advancing our understanding of cellular regulation and the intricate balance of cellular processes that maintain cellular integrity and function.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Brefeldin A | 20350-15-6 | sc-200861C sc-200861 sc-200861A sc-200861B | 1 mg 5 mg 25 mg 100 mg | ¥338.00 ¥587.00 ¥1376.00 ¥4140.00 | 25 | |
破坏ARF依赖的GEF活性,从而间接影响Rab GTPase在囊泡运输中的作用。 | ||||||
Lovastatin | 75330-75-5 | sc-200850 sc-200850A sc-200850B | 5 mg 25 mg 100 mg | ¥316.00 ¥993.00 ¥3746.00 | 12 | |
抑制HMG-CoA还原酶,影响异戊二烯生物合成,间接影响Rab GTPase′的异戊二烯化。 | ||||||
Gliotoxin | 67-99-2 | sc-201299 sc-201299A | 2 mg 10 mg | ¥1478.00 ¥4355.00 | 1 | |
改变蛋白质的异戊二烯化,可能影响Rab GTPase的膜结合。 | ||||||
Zoledronic acid, anhydrous | 118072-93-8 | sc-364663 sc-364663A | 25 mg 100 mg | ¥1015.00 ¥2832.00 | 5 | |
抑制法呢基焦磷酸合成酶,可能影响Rab GTPase′的异戊二烯化和功能。 | ||||||
GW 5074 | 220904-83-6 | sc-200639 sc-200639A | 5 mg 25 mg | ¥1196.00 ¥4705.00 | 10 | |
Raf激酶抑制剂,可能对Rab蛋白信号通路产生非靶向效应。 | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | ¥2053.00 ¥7818.00 | 88 | |
Y-27632是ROCK(Rho相关蛋白激酶)的选择性抑制剂。ROCK参与肌动蛋白细胞骨架的构建,影响细胞过程,如Rab GTPase起作用的囊泡运输。通过抑制ROCK,Y-27632可以改变细胞骨架动力学,从而影响Rab GTPase介导的囊泡运输和膜融合事件。 | ||||||
Gö 6983 | 133053-19-7 | sc-203432 sc-203432A sc-203432B | 1 mg 5 mg 10 mg | ¥1162.00 ¥3306.00 ¥5246.00 | 15 | |
Gö6983是蛋白激酶C(PKC)异构体的广谱抑制剂。PKC在多种细胞过程中发挥作用,包括涉及膜动力学和囊泡运输的细胞过程。通过抑制PKC活性,Gö6983可以影响这些细胞过程,间接影响Rab GTPase′在膜运输中的作用。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | ¥733.00 ¥3012.00 | 257 | |
SP600125是JNK(c-Jun N-末端激酶)的抑制剂,JNK是MAPK信号传导通路的一个组成部分。通过抑制JNK,SP600125可以影响调控囊泡形成和运输的信号传导通路,从而可能影响Rab GTPase′在这些过程中的作用。 | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | ¥293.00 ¥1038.00 ¥1354.00 ¥3497.00 ¥5641.00 ¥10244.00 ¥20545.00 | 46 | |
染料木素是一种具有广泛特异性的酪氨酸激酶抑制剂。酪氨酸激酶参与调控内吞作用和囊泡运输的信号通路,而Rab GTPase在这些过程中活跃。通过抑制这些激酶,染料木素可以调节信号通路,从而可能影响Rab GTPase在囊泡动力学中的活性。 |