Liprin α4 inhibitors are a class of small molecules that target Liprin α4, a member of the Liprin family of scaffolding proteins. Liprin proteins are involved in the organization of cellular signaling networks, particularly in synapse formation and maintenance, as well as in cell adhesion and migration. Liprin α4 specifically plays a crucial role in the regulation of protein complexes that are essential for intracellular trafficking and signaling pathways. By inhibiting Liprin α4, these compounds can interfere with its scaffolding functions, which affects the assembly of protein complexes and alters various signaling cascades within the cell. This inhibition can lead to changes in cellular organization, migration, and overall cellular communication.
Structurally, Liprin α4 inhibitors typically interact with the protein through specific binding sites that affect its conformation and activity. The structural diversity of these inhibitors allows for a range of specificities and affinities, depending on the compound's interaction with the different domains of Liprin α4. Some inhibitors may work by preventing the protein from interacting with its partners, such as those involved in cytoskeletal dynamics or vesicular transport, while others may induce conformational changes that disrupt the protein's scaffolding capacity. These compounds are useful for probing the biological functions of Liprin α4, allowing researchers to dissect the molecular mechanisms by which Liprin α4 contributes to cellular processes such as morphogenesis, polarization, and signal transduction pathways in various cell types.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | ¥3159.00 | 4 | |
这种DNA甲基转移酶抑制剂可能导致Liprin α4基因启动子甲基化不足,从而降低其转录活性,并随之降低蛋白水平。 | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | ¥1681.00 ¥5303.00 ¥6995.00 ¥13527.00 ¥23579.00 | 33 | |
Trichostatin A可抑制组蛋白去乙酰化酶,导致Liprin α4基因周围的乙酰化组蛋白增加。这种变化可能会对基因转录物产生不利影响,从而降低Liprin α4的表达。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | ¥699.00 ¥1749.00 ¥3610.00 | 233 | |
通过特异性抑制mTOR通路,雷帕霉素可导致依赖帽的mRNA翻译总体减少,包括Liprin α4的mRNA。这将导致Liprin α4蛋白的合成减少。 | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | ¥1489.00 ¥12004.00 | 115 | |
尽管硼替佐米是一种蛋白酶体抑制剂,但它对蛋白质稳态的影响可能会导致细胞应激反应,包括某些蛋白质的下调,其中可能包括Liprin α4,这是细胞试图恢复稳态的更广泛反应的一部分。 | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | ¥880.00 ¥2866.00 | 41 | |
黄酮哌啶醇可抑制依赖细胞周期蛋白的激酶,从而导致细胞周期停滞。这种细胞周期停滞反过来又会下调参与细胞周期进展的蛋白质的表达,可能包括脂蛋白α4。 | ||||||
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 | |
放线菌素D插入DNA并阻断RNA聚合酶的延伸阶段,这可能导致包括Liprin α4在内的总mRNA产量下降,从而降低其蛋白质表达。 | ||||||
Pladienolide B | 445493-23-2 | sc-391691 sc-391691B sc-391691A sc-391691C sc-391691D sc-391691E | 0.5 mg 10 mg 20 mg 50 mg 100 mg 5 mg | ¥3272.00 ¥62863.00 ¥122015.00 ¥282050.00 ¥733330.00 ¥31375.00 | 63 | |
这种剪接抑制剂可能会破坏脂联蛋白α4基因前mRNA转录的正常剪接,从而可能导致非功能性mRNA的产生或用于翻译的成熟mRNA数量显著减少。 | ||||||
Tetracycline | 60-54-8 | sc-205858 sc-205858A sc-205858B sc-205858C sc-205858D | 10 g 25 g 100 g 500 g 1 kg | ¥699.00 ¥1038.00 ¥2990.00 ¥4614.00 ¥7017.00 | 6 | |
它与细菌核糖体的 30S 亚基结合,通过阻断氨基酰-tRNA 与核糖体接受位点的连接来抑制蛋白质的合成。在研究环境中,它可能被用来抑制真核蛋白质的合成,包括抑制脂蛋白 α4,产生脱靶效应。 | ||||||
Sofosbuvir | 1190307-88-0 | sc-482362 | 25 mg | ¥1613.00 | 1 | |
索非布韦的主要用途是作为抗病毒药物,作用于病毒RNA聚合酶,但它可能会对细胞造成压力,间接导致多种细胞蛋白的下调,包括脂联蛋白α4,因为细胞会重新分配资源。 |