Date published: 2025-10-10

021-6093-6350

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eIF3M 抑制因子

eIF3M inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the eukaryotic translation initiation factor 3 subunit M (eIF3M). eIF3M is a component of the eIF3 complex, which is a crucial player in the initiation phase of eukaryotic translation. The eIF3 complex is the largest and most complex of the translation initiation factors, composed of multiple subunits, including eIF3M. This complex plays a critical role in the recruitment of the small ribosomal subunit to the mRNA, the scanning of the mRNA for the start codon, and the assembly of the translation machinery. Inhibiting eIF3M can disrupt the overall function of the eIF3 complex, thereby impeding the translation initiation process. This makes eIF3M inhibitors important tools in research for studying the specific role of this subunit in translation and its broader impact on protein synthesis.

The study of eIF3M inhibitors provides valuable insights into the mechanistic aspects of translation initiation. By selectively inhibiting eIF3M, researchers can dissect the specific contributions of this subunit to the eIF3 complex's function and its interaction with other components of the translation machinery. This approach allows scientists to explore how eIF3M influences the regulation of gene expression at the translational level, as well as its involvement in various cellular processes that depend on efficient protein synthesis. Furthermore, eIF3M inhibitors can help identify potential regulatory networks that modulate the activity of the eIF3 complex, offering a deeper understanding of how cells control protein production under different physiological conditions. Overall, eIF3M inhibitors are essential tools for advancing our knowledge of translation initiation and the complex molecular mechanisms that govern this fundamental process in eukaryotic cells.

関連項目

Items 11 to 14 of 14 total

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产品名称CAS #产品编号数量价格应用排名

Camptothecin

7689-03-4sc-200871
sc-200871A
sc-200871B
50 mg
250 mg
100 mg
¥643.00
¥2053.00
¥1038.00
21
(2)

喜树碱(Camptothecin)对拓扑异构酶I的抑制作用可能会导致DNA受损,从而降低对RNAi过程的重视程度,并随之降低eIF2C2的表达。

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
¥429.00
¥654.00
¥1151.00
¥2279.00
8
(1)

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。

Silvestrol

697235-38-4sc-507504
1 mg
¥10379.00
(0)

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

84573-16-0sc-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
(1)

另一种天然化合物存在于多种植物中,如Aglaia属植物,具有强效的EIF4AI抑制活性。