Date published: 2025-11-4

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NARG2 Inhibitors

Chemical inhibitors of NARG2 act through various mechanisms to impede its activity, primarily by disrupting signaling pathways that regulate its function. Wortmannin and LY294002 are both inhibitors of PI3K, an upstream regulator of the Akt signaling pathway, which is crucial for the proper regulation of NARG2. By inhibiting PI3K, these chemicals prevent the activation of Akt, thus leading to a decrease in NARG2 activity. Similarly, Rapamycin and PP242 target mTOR, a component further downstream in the Akt pathway. The inhibition of mTOR by these chemicals results in a disruption of Akt signaling, which is necessary for NARG2's role in cellular functions. PP242, in particular, is known for its selective inhibition of both mTORC1 and mTORC2 complexes, thus exerting a more comprehensive inhibition of the pathway and subsequent NARG2 activity. Additional chemicals such as Spautin-1 act on autophagy-related proteins like Beclin-1, which is also regulated by Akt, leading to indirect inhibition of NARG2. MK-2206, Perifosine, and Triciribine directly target Akt to prevent its activation and phosphorylation, critical steps required for NARG2 to exert its function within the cell. Torin 1, like PP242, is an inhibitor of mTOR and affects both mTORC1 and mTORC2 complexes, leading to dampened Akt signaling and reduced activity of NARG2. Palomid 529 disrupts the Akt pathway by dual inhibition of PI3K and mTOR, while KU-0063794's specific inhibition of mTORC1 and mTORC2 complexes leads to decreased Akt signaling, culminating in the suppression of NARG2 activity. Lastly, SAR405 inhibits Vps34, which is part of the PI3K-III pathway involved in the regulation of autophagy by Akt, and this inhibition can lead to a decrease in the activity of NARG2. Each chemical executes a strategic blockade at various junctures of the signaling pathways that NARG2 relies on, ensuring the comprehensive inhibition of its function within cells.

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