Date published: 2025-9-11

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CCDC68 Inhibitors

Chemical inhibitors of CCDC68 can exert their inhibitory effects through various cellular pathways by targeting specific enzymes and kinases that regulate the function and activity of CCDC68 within the cell. Staurosporine, a broad-spectrum protein kinase inhibitor, can inhibit CCDC68 through its potential role in phosphorylation events that regulate CCDC68's function, particularly in cell signaling. Similarly, Wortmannin and LY294002, both phosphoinositide 3-kinases (PI3K) inhibitors, can disrupt the PI3K/Akt signaling pathway, which is often implicated in the regulation of proteins like CCDC68. Rapamycin, an mTOR pathway inhibitor, can also suppress the activity of CCDC68 by interfering with downstream effects of mTOR signaling that might otherwise contribute to the functional regulation of CCDC68.

Furthermore, U0126 and PD98059, both MEK inhibitors, can inhibit CCDC68 by hindering the MEK/ERK pathway, which is known to have roles in cell cycle regulation where CCDC68 may be implicated. SB203580, as a p38 MAP Kinase inhibitor, and SP600125, a JNK inhibitor, can inhibit CCDC68 by blocking the p38 MAPK and JNK signaling pathways, respectively, which are involved in cellular stress responses and may intersect with CCDC68's regulatory functions. Inhibition of Bruton's tyrosine kinase by LFM-A13 can inhibit CCDC68 by disrupting Btk-dependent signaling pathways that could involve CCDC68. Dasatinib and PP2, both Src family kinase inhibitors, can inhibit CCDC68 by targeting Src family kinases that are likely to phosphorylate CCDC68, thereby controlling its activity. Lastly, Gefitinib, an EGFR inhibitor, can inhibit CCDC68 by blocking the EGFR signaling pathway, which may play a crucial role in the regulation of CCDC68's function within various cellular processes. Each of these inhibitors acts on a specific pathway or enzyme that has a connection to the cellular functions of CCDC68, providing a targeted approach to inhibiting this protein.

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