Date published: 2025-9-13

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GCN1L1 Activators

GCN1L1, also known as GCN1, is implicated in a series of critical cellular processes, especially in protein synthesis under stress conditions. The protein's role in these pathways gives rise to a plethora of potential indirect activators that can modulate its function through various cellular signals. Chemicals such as Forskolin and Isoproterenol, both of which target the cAMP pathways, are examples of compounds that can indirectly influence the cellular contexts in which GCN1L1 operates. Lithium chloride, an activator of the Wnt signaling pathway, may also provide an environment conducive to the function of GCN1L1 in cells.

Similarly, the MAPK/ERK pathway, which can be modulated by U0126 and PD98059, both MEK inhibitors, may intersect with GCN1L1's functionalities. LY294002 and Wortmannin, known PI3K inhibitors, suggest a connection between the PI3K/AKT pathway and GCN1L1, highlighting its wide-reaching relevance in cellular dynamics. Rapamycin, an mTOR inhibitor, underscores the importance of GCN1L1 in cellular growth and protein synthesis pathways, and the potential influence this compound can have on the protein's role. PMA, which activates Protein Kinase C, further demonstrates the expansive cellular signaling network that GCN1L1 might be associated with.

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