Date published: 2025-9-17

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GAGE2C Inhibitors

GAGE2C inhibitors encompass a range of chemical compounds that exert their effects by impeding various biochemical pathways, ultimately leading to the decreased activity of GAGE2C. These inhibitors work by targeting upstream kinases, thus preventing the phosphorylation that is essential for the proper functioning of GAGE2C. Specific kinase inhibitors interfere with the MAPK/ERK and PI3K/AKT pathways, which are crucial for the phosphorylation state and subsequent activation of proteins, including GAGE2C. By inhibiting MEK, the MAPK/ERK pathway is dampened, resulting in the alteration of the phosphorylation status of GAGE2C, which is a prerequisite for its activity. Similarly, by hindering p38 MAPK, the compounds indirectly lead to the reduction of GAGE2C activity, as this pathway is known to regulate a variety of proteins through phosphorylation.

Further inhibitory actions include the disruption of protein synthesis pathways, particularly through the inhibition of mTOR, which plays a pivotal role in the synthesis and stability of many proteins, including GAGE2C. In addition, interference with JNK signaling has an impact on transcription factors that may control the expression of GAGE2C. Other mechanisms involve the alteration of histone acetylation states, thereby influencing the gene expression profile, including that of GAGE2C. Chemicals that inhibit HIF-1α under hypoxic conditions can also lead to the downregulation of GAGE2C, which is responsive to such environmental stress signals. Moreover, the modulation of protein kinase C (PKC) activity results in the decreased phosphorylation of proteins within the same signaling cascade as GAGE2C, thus reducing its functional activity.

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