Date published: 2025-10-11

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AI314180 Inhibitors

AI314180 inhibitors are chemical compounds that can directly or indirectly influence the function of AI314180, a protein involved in the phosphoinositide 3-kinase (PI3K) and Akt signaling pathway. For instance, inhibitors like Wortmannin, LY294002, Quercetin, PI-103, and PX-866 can disrupt the activation of Akt by inhibiting PI3K, an upstream regulator of Akt. PI3K is a lipid kinase that phosphorylates phosphatidylinositol 4,5-bisphosphate to generate phosphatidylinositol 3,4,5-trisphosphate, a secondary messenger that activates Akt. By inhibiting PI3K, these compounds reduce the generation of phosphatidylinositol 3,4,5-trisphosphate, thereby reducing the activation of Akt. As Akt is involved in the phosphorylation and activation of AI314180, disrupting Akt activation leads to decreased functional activity of AI314180.

Moreover, compounds like Wortmannin, LY294002, Quercetin, PI-103, and PX-866, which inhibit PI3K, can disrupt the phosphorylation and activation of Akt. Akt, a crucial component of the PI3K/Akt pathway, is responsible for phosphorylating and activating AI314180. By inhibiting PI3K, these compounds can elicit a decrease in Akt activation, which in turn negatively impacts the activation of AI314180. Similarly, compounds like AKT inhibitor VIII, Perifosine, Triciribine, GSK690693, MK-2206, and API-2 directly inhibit Akt. Akt, also known as protein kinase B, plays a central role in the PI3K/Akt pathway. By inhibiting Akt, these compounds can directly decrease the phosphorylation and activation of AI314180. Lastly, inhibitors like Rapamycin and PI-103 disrupt the mTOR pathway downstream of Akt. mTOR, a downstream target of Akt, plays a critical role in cell growth and proliferation. By inhibiting mTOR, these compounds can disrupt the activation and function of AI314180.

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