SMCR8 activators are chemical compounds that augment the functional activity of SMCR8 by facilitating autophagy, a cellular degradation pathway crucial for maintaining cellular homeostasis. Compounds like Forskolin, AICAR, Metformin, and Rapamycin function through metabolic and nutrient-sensing pathways to enhance autophagy. For instance, Forskolin increases cAMP levels, which can activate PKA, leading to the phosphorylation of autophagy-related substrates and the enhancement of SMCR8 activity within these pathways. AICAR and Metformin exert their effects by activating AMPK, a central regulator of cellular energy homeostasis, which subsequently promotes autophagic processes involving SMCR8. Rapamycin, by inhibiting the mTOR pathway, a key negative regulator of autophagy, allows for the upregulation of autophagic pathways, consequently potentiating the role of SMCR8.
Moreover, compounds such as Spermidine, Lithium Chloride, and Nicotinamide target the autophagic machinery at different stages and through various mechanisms, which leads to the enhanced activity of SMCR8. Spermidine's ability to induce autophagy through acetyltransferase inhibition, Lithium Chloride's effect via inositol monophosphatase inhibition, and Nicotinamide's role in sirtuin inhibition all contribute to the functional enhancement of SMCR8. Additionally, LY294002, Resveratrol, Curcumin, 2-Deoxy-D-glucose, and Trehalose each modulate the autophagic pathway through unique interventions such asPI3K inhibition, sirtuin activation, AMPK activation, glycolysis inhibition, and direct autophagy induction, respectively. These activators, through distinct cellular actions, culminate in the promotion of autophagic pathways in which SMCR8 operates, enhancing its activity and role in cellular autophagy without directly increasing its expression or affecting its gene regulation.
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