Date published: 2025-9-26

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E2F-5 Inhibitors

E2F-5 Inhibitors comprise a group of chemical compounds that indirectly modulate the activity of E2F-5, a transcription factor critical for cell cycle regulation, cell growth, and proliferation. These inhibitors act by targeting specific pathways and cellular mechanisms that intersect with E2F-5's function, resulting in the inhibition or modulation of E2F-5 activity. One prominent member of this class is Palbociclib, a CDK4/6 inhibitor that indirectly influences E2F-5 by blocking the CDK4/6 pathway. E2F-5's transcriptional activity is tightly regulated through phosphorylation by CDKs, and Palbociclib disrupts this regulation, thereby modulating E2F-5-mediated cell cycle progression. Nutlin-3 is another E2F-5 Inhibitor that indirectly modulates E2F-5 by stabilizing p53. E2F-5 is known to interact with p53, and Nutlin-3's action results in increased p53 levels, which can suppress E2F-5's transcriptional activity and its role in cell cycle control.

Additionally, inhibitors like AZD8055, Selumetinib, LY294002, and others target the mTOR, MAPK/ERK, and PI3K/Akt pathways, all of which can intersect with E2F-5's function. By modulating these pathways, these inhibitors indirectly influence E2F-5 expression and activity, providing valuable tools for understanding and manipulating E2F-5 in cellular processes. In conclusion, E2F-5 Inhibitors represent a class of chemical compounds that indirectly modulate E2F-5 by targeting pathways and cellular mechanisms intersecting with E2F-5's function. These inhibitors contribute to our understanding of E2F-5's role in cell cycle regulation and provide insights into research avenues for controlling cell growth and proliferation, although further investigation is required to elucidate their specific mechanisms of action and applications.

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