Date published: 2025-9-15

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APC15 Inhibitors

APC15 inhibitors encompass a diverse chemical class that is defined not by direct interaction with the APC15 protein itself, but rather by their ability to modulate the cellular processes and signaling pathways in which APC15 is involved. These chemicals exert their effects on processes such as the cell cycle, mitosis, and DNA damage response, all of which are integral to the proper functioning of the anaphase-promoting complex/cyclosome (APC/C), with which APC15 is associated.

Proteasome inhibitors like MG-132 interfere with the degradation of cell cycle regulators, thereby affecting APC15 indirectly by altering the turnover of proteins that are substrates of the APC/C, potentially leading to cell cycle arrest. Similarly, mitotic inhibitors such as Nocodazole disrupt microtubule dynamics, which can impede the progression of mitosis and inadvertently affect the function of APC15 in cell cycle regulation.The chemical class referred to as APC15 inhibitors is quite heterogeneous, encompassing various mechanisms of action that all converge on the indirect modulation of APC15's activity through different aspects of cellular regulation. This collection of inhibitors does not interact with APC15 directly; instead, their actions perturb the cellular milieu and the orchestrated series of events in which APC15 plays a part. By influencing the stability and activity of proteins and complexes that work in concert with APC15, these chemicals effectively modulate the protein's function. This modulation can manifest in varied impacts on the cell cycle and other cellular processes, reflecting the intricate interplay between these compounds and the biological pathways they affect.

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