Date published: 2025-9-11

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TBC1D7 Activators

The chemical class termed TBC1D7 Activators comprises a range of compounds that could potentially influence the activity of TBC1D7 indirectly. TBC1D7 is a component of the Tsc-TBC1D7 complex, playing a significant role in the regulation of mTORC1 signaling, a key pathway in controlling cell growth, proliferation, and metabolism. The modulation of TBC1D7 is linked to an intricate network of signaling pathways and cellular regulatory mechanisms. Compounds such as Rapamycin, Metformin, and AICAR, known for their roles in modulating mTOR and AMPK pathways, demonstrate the potential to influence TBC1D7 activity. Rapamycin's inhibitory effect on mTORC1 and Metformin's and AICAR's activation of AMPK highlight the critical interplay between energy metabolism and cell growth regulation pathways in which TBC1D7 is involved. Additionally, insulin, a central regulator of glucose metabolism, might also impact TBC1D7 through insulin signaling pathways, indicating the multifaceted nature of metabolic regulation and its impact on TBC1D7.

Furthermore, the inclusion of compounds that affect broader cellular signaling and regulatory mechanisms, such as Resveratrol, Pioglitazone, Forskolin, and Curcumin, reflects the complex interplay between different signaling molecules and TBC1D7. These compounds, through their diverse effects on SIRT1 activation, lipid metabolism, cAMP levels, and various signaling pathways, provide insights into the indirect mechanisms through which TBC1D7 can be modulated. The role of dexamethasone, LY294002, and PD98059 in influencing glucocorticoid, PI3K-Akt, and MAPK/ERK pathways respectively, along with Sodium Butyrate's impact on epigenetic regulation, further underscores the interconnected nature of cellular signaling in regulating key proteins like TBC1D7.

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