eIF2Bδ Inhibitors are a class of chemical compounds that specifically target the δ subunit of eukaryotic initiation factor 2B (eIF2B), a critical regulator in the process of protein synthesis. eIF2B is a guanine nucleotide exchange factor (GEF) that plays a pivotal role in the initiation of translation by catalyzing the exchange of GDP for GTP on eIF2, a process essential for the formation of the translation initiation complex. The eIF2B complex is composed of five subunits (α, β, γ, δ, and ε), with each subunit contributing to the overall function and regulation of the complex. The δ subunit, in particular, is crucial for the structural stability and proper assembly of the eIF2B complex, as well as for the interaction with eIF2.
Inhibitors that target eIF2Bδ disrupt the normal function of eIF2B, leading to a decrease in its GEF activity. This disruption impacts the global regulation of protein synthesis within the cell, as the reduced activity of eIF2B results in decreased levels of active eIF2-GTP, ultimately leading to a slowdown in translation initiation. By inhibiting eIF2Bδ, researchers can investigate the broader regulatory mechanisms of protein synthesis and how cells respond to various stress conditions that affect translation. These inhibitors are valuable tools for studying the cellular responses to changes in translation rates, the role of eIF2B in maintaining proteostasis, and the intricate signaling pathways that regulate protein synthesis in response to environmental cues. Furthermore, eIF2Bδ inhibitors provide insights into the complex interplay between different subunits of the eIF2B complex and their individual contributions to the regulation of translation, making them an essential resource in the field of molecular biology and biochemistry.
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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 | |
阿霉素对DNA的损伤可能会导致细胞优先考虑DNA修复而不是常规功能,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 | |
喜树碱对拓扑异构酶I的抑制作用可导致DNA损伤,从而可能降低对RNAi过程的重视程度,并导致eIF2C2表达降低。 | ||||||
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,包括降低eIF2C2的稳定性或合成。 | ||||||
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,可通过抑制蛋白质翻译间接影响EIF3ε。它具有抗癌治疗潜力,目前正在进行相关研究。 | ||||||
Silvestrol | 697235-38-4 | sc-507504 | 1 mg | ¥10379.00 | ||
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,具有强大的EIF4AI抑制活性。 | ||||||
4E1RCat | 328998-25-0 | sc-361085 sc-361085A | 10 mg 50 mg | ¥2132.00 ¥8992.00 | ||
一种人工合成的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,从而阻止翻译开始。 |