Date published: 2025-9-14

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CC2D2A Inhibitors

Chemical inhibitors of CC2D2A can interfere with its function in a variety of ways, as each chemical targets different aspects of the cellular pathways that are essential for the proper functioning of CC2D2A. For instance, Alsterpaullone and SB216763 both target GSK-3β, a kinase that plays a pivotal role in phosphorylating proteins within the pathways that CC2D2A operates. By inhibiting this kinase, these chemicals disrupt critical processes necessary for ciliogenesis, which is closely related to the normal function of CC2D2A. Similarly, Indirubin-3'-monoxime acts as a dual inhibitor of CDKs and GSK-3β, impeding the regulation of the cell cycle and ciliogenesis, and thereby affecting the function of CC2D2A. Roscovitine and Purvalanol A also target CDKs, which are integral in controlling cell cycle progression, a process that must be finely tuned for ciliogenesis to proceed normally, thus impacting the functionality of CC2D2A.

Additionally, Pifithrin-μ inhibits Heat Shock Protein 70 (HSP70), which assists in the proper folding and stabilization of proteins, including those involved in the pathways where CC2D2A is active. This inhibition could lead to a functional disruption of CC2D2A due to the misfolding or instability of ciliary proteins. SP600125, by inhibiting JNK, affects signaling pathways that regulate various cellular processes, including those involving CC2D2A. LY294002, a PI3K inhibitor, disrupts signaling pathways that are crucial for CC2D2A's role in ciliogenesis. Rapamycin inhibits mTOR, which is part of the pathway regulating cell growth and proliferation, processes that are crucial for ciliogenesis and thus the function of CC2D2A. Cyclopamine targets the Hedgehog signaling pathway, which is vital for ciliogenesis and the ciliary function that CC2D2A supports. Lastly, 5-Iodotubercidin and Nocodazole impact ciliogenesis by modulating cAMP levels and disrupting microtubule polymerization, respectively, both of which are essential for maintaining the structure and function of cilia, thereby influencing the function of CC2D2A.

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