eIF5A1 Inhibitors are a specialized class of chemical compounds that target and inhibit the activity of eukaryotic initiation factor 5A1 (eIF5A1), a highly conserved protein involved in the regulation of translation. eIF5A1 is unique because it is the only known protein to undergo post-translational modification by hypusination, a process that is crucial for its function in promoting the synthesis of specific proteins, particularly those involved in cell proliferation, differentiation, and stress responses. By inhibiting eIF5A1, researchers can study the detailed mechanisms of translation elongation and the role of hypusinated eIF5A1 in various cellular processes, including the synthesis of proteins that are otherwise challenging to produce or regulate within the cell.
The inhibition of eIF5A1 is particularly valuable for exploring its involvement in the regulation of proteins with proline-rich sequences, which are known to be critical for the control of cell cycle progression and apoptosis. eIF5A1 Inhibitors provide a powerful tool for dissecting the molecular pathways that rely on these specific proteins, allowing scientists to gain insights into how cells regulate essential functions like growth, division, and response to environmental stressors. Furthermore, these inhibitors offer a way to study the broader impact of translation control on cellular homeostasis and the maintenance of protein quality. By modulating eIF5A1 activity, researchers can explore how the balance of protein synthesis and degradation is maintained in the cell and how disruptions to this balance can lead to various cellular outcomes. Overall, eIF5A1 Inhibitors serve as a critical resource for advancing our understanding of the complex network of interactions that govern translation and protein synthesis in eukaryotic cells.
関連項目
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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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Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | ¥1952.00 ¥4716.00 | 43 | |
阿霉素(Doxorubicin)对DNA的损伤可能会导致细胞优先修复DNA,而忽略常规功能,从而抑制RNAi机制并降低eIF2C2水平。 | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | ¥643.00 ¥2053.00 ¥1038.00 | 21 | |
喜树碱(Camptothecin)对拓扑异构酶I的抑制作用可能会导致DNA损伤,从而降低对RNAi过程的重视程度,并随之降低eIF2C2的表达。 | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | ¥429.00 ¥654.00 ¥1151.00 ¥2279.00 | 8 | |
通过抑制Hsp90,格尔德霉素可能会破坏与RNAi相关的蛋白质的稳定性,这可能会导致eIF2C2的稳定性或合成降低。 | ||||||
MLN7243 | 1450833-55-2 | sc-507338 | 5 mg | ¥3836.00 | ||
TAK-243是一种小分子泛素激活酶(UAE)抑制剂,通过抑制蛋白质翻译间接影响EIF3ε。它已被研究用于抗癌治疗。 | ||||||
Silvestrol | 697235-38-4 | sc-507504 | 1 mg | ¥10379.00 | ||
一种从Aglaia foveolata植物中分离出的天然化合物,因其对EIF4AI的强效抑制作用而闻名。 | ||||||
Rocaglamide | 84573-16-0 | sc-203241 sc-203241A sc-203241B sc-203241C sc-203241D | 100 µg 1 mg 5 mg 10 mg 25 mg | ¥3046.00 ¥5246.00 ¥18130.00 ¥27618.00 ¥59106.00 | 4 | |
另一种天然化合物存在于多种植物中,如Aglaia属植物,对EIF4AI有很强的抑制作用。 | ||||||
4E1RCat | 328998-25-0 | sc-361085 sc-361085A | 10 mg 50 mg | ¥2132.00 ¥8992.00 | ||
一种合成的EIF4AI抑制剂,旨在破坏eIF4F复合物,从而抑制依赖帽的翻译。 | ||||||
eIF4E/eIF4G Interaction Inhibitor, 4EGI-1 | 315706-13-9 | sc-202597 | 10 mg | ¥2933.00 | 14 | |
一种小分子,可破坏eIF4E-eIF4G相互作用,从而阻止翻译起始。 |