Date published: 2025-9-18

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4932443I19Rik Inhibitors

The chemical class termed Cfap97d2 Inhibitors refers to a heterogeneous group of compounds that can indirectly influence the function of the protein Cfap97d2 by modulating various cellular signaling pathways and processes. The activity of Cfap97d2 can be altered by changes in the cellular environment that are induced by these compounds, which interfere with cellular signaling or structural components at different points.

For example, inhibitors like Chlorpromazine and Genistein can modify receptor-mediated signaling or kinase activity, respectively, leading to alterations in signaling networks that Cfap97d2 may be part of. Drugs that affect the cell's structural integrity, such as Colchicine and Nocodazole, disrupt microtubule dynamics, which is essential for processes such as cell division and intracellular transport, potentially affecting the distribution or function of Cfap97d2. Compounds like Forskolin, by increasing cAMP levels, and LY294002 and Wortmannin, by inhibiting PI3K, can result in broad changes in cellular signaling pathways, which may have downstream effects on Cfap97d2. Staurosporine, as a broad-spectrum kinase inhibitor, and specific kinase inhibitors like Imatinib, PD98059, and Rapamycin, target key nodes in cellular signaling networks, which can have cascading effects on various processes within the cell, including those associated with Cfap97d2.

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