Date published: 2025-12-24

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SCML4 Activators

Chemical activators of SCML4 include a variety of compounds that induce the activation of this protein through different biochemical pathways. Epigallocatechin gallate (EGCG) and Metformin, for instance, both activate the AMP-activated protein kinase (AMPK) pathway. Once AMPK is activated, it can directly phosphorylate SCML4, which enhances its activity within the cell. Similarly, AICAR, an analog of AMP, also activates AMPK leading to the phosphorylation of SCML4 as part of the cellular energy regulation process. Forskolin and Dibutyryl-cAMP, on the other hand, increase cyclic AMP (cAMP) levels within the cell. This rise in cAMP activates protein kinase A (PKA), which then can phosphorylate SCML4, thereby activating it within the cAMP signaling pathway.

Other compounds affect SCML4 through different mechanisms. Ionomycin, by increasing the intracellular calcium concentration, activates the calcium/calmodulin-dependent protein kinases (CaMKs). These kinases then phosphorylate SCML4 within the calcium signaling pathway. Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which also leads to the phosphorylation and activation of SCML4 within the PKC signaling cascade. Resveratrol, through the activation of Sirtuin 1, can lead to the activation of SCML4 via deacetylation. Spermidine induces autophagy by inhibiting the acetyltransferase EP300, which may result in the activation of SCML4 through a series of deacetylation events. Additionally, retinoic acid, via its receptor, can activate the MAPK signaling pathway, leading to the activation of SCML4 through phosphorylation. Curcumin's activation of the JNK pathway similarly results in the phosphorylation and activation of SCML4. Lastly, Lithium chloride inhibits GSK-3, which in turn activates the Wnt signaling pathway, potentially leading to the stabilization and regulation of SCML4's phosphorylation state, resulting in its activation.

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