Date published: 2025-9-11

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eIF3M Inhibitoren

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.

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ProduktCAS #Katalog #MengePreisReferenzenBewertung

Camptothecin

7689-03-4sc-200871
sc-200871A
sc-200871B
50 mg
250 mg
100 mg
$57.00
$182.00
$92.00
21
(2)

Die Hemmung der Topoisomerase I durch Camptothecin kann zu DNA-Schäden führen, was wiederum dazu führen kann, dass der Fokus auf RNAi-Prozesse verringert wird und die eIF2C2-Expression sinkt.

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
$38.00
$58.00
$102.00
$202.00
8
(1)

Durch die Hemmung von Hsp90 kann Geldanamycin Proteine destabilisieren, die mit RNAi in Verbindung stehen, was zu einer Abnahme der eIF2C2-Stabilität oder -Synthese führen könnte.

Silvestrol

697235-38-4sc-507504
1 mg
$920.00
(0)

Ein natürlicher Wirkstoff, der aus der Pflanze Aglaia foveolata isoliert wurde und für seine starke Hemmung von EIF4AI bekannt ist.

Rocaglamide

84573-16-0sc-203241
sc-203241A
sc-203241B
sc-203241C
sc-203241D
100 µg
1 mg
5 mg
10 mg
25 mg
$270.00
$465.00
$1607.00
$2448.00
$5239.00
4
(1)

Ein weiterer natürlicher Wirkstoff, der in mehreren Pflanzen, wie z. B. der Gattung Aglaia, vorkommt und eine starke EIF4AI-hemmende Wirkung hat.