Date published: 2025-9-15

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C17orf63 Activators

The C17orf63 activators constitute a diverse assembly of chemical compounds, each intricately influencing the expression and activity of C17orf63. A769662, recognized as a direct activator, engages AMP-activated protein kinase (AMPK) to positively modulate C17orf63 within cellular contexts. AICAR, in the activator repertoire, operates indirectly by stimulating AMPK, providing an alternative avenue for C17orf63 modulation through this crucial cellular kinase. GW7647, identified as a direct activator, exerts its effects on C17orf63 by activating peroxisome proliferator-activated receptor delta (PPARδ). This activation establishes a direct link between GW7647 and the modulation of C17orf63 expression and activity within the cellular environment. GSK2334470, on the other hand, operates indirectly by inhibiting 3-phosphoinositide-dependent protein kinase 1 (PDK1), contributing to C17orf63 activation through the modulation of downstream effectors. SC79, functioning as an indirect activator, activates Akt, thereby influencing cellular events that contribute to C17orf63 activation in a context-dependent manner. The inclusion of 2-Deoxyglucose in the activator repertoire showcases an indirect mechanism involving glycolysis inhibition, which influences downstream events positively regulating C17orf63 expression and activity.

STO-609, a compound in the activator list, indirectly activates C17orf63 by inhibiting calcium/calmodulin-dependent protein kinase kinase (CaMKK), impacting downstream effectors and contributing to C17orf63 activation. Berberine, another compound, indirectly influences C17orf63 by inhibiting mammalian target of rapamycin (mTOR), linking mTOR signaling to the modulation of C17orf63 within the cellular context. Direct activator A769829 engages peroxisome proliferator-activated receptor alpha (PPARα) to positively regulate C17orf63 expression and activity, establishing a specific connection between A769829 and C17orf63 modulation. Halofuginone, in the activator repertoire, operates indirectly by inhibiting transforming growth factor-beta (TGF-β), influencing downstream effectors and contributing to C17orf63 activation. In conclusion, the C17orf63 activators represent a sophisticated array of chemical compounds, each with a specific mode of action influencing C17orf63 expression and activity within cellular contexts.

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