Date published: 2025-9-15

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SASPase Activators

SASPase activators comprise a spectrum of chemical compounds that enhance the activity of SASPase by interfacing with various cellular signaling pathways. Forskolin, by raising intracellular cAMP levels, indirectly activates PKA, which may phosphorylate SASPase, thereby amplifying its activity in skin processes. Curcumin, through NF-κB pathway modulation, potentially increases SASPase activity by mitigating inflammatory signaling that can suppress SASPase functions. Resveratrol, through SIRT1 activation, might encourage SASPase activity enhancement via the deacetylation of proteins that regulate SASPase-related cellular mechanisms. Retinoic Acid's influence on gene expression is another avenue through which SASPase activity may be upregulated, particularly by promoting the differentiation of keratinocytes, the site of SASPase's functional relevance.

Continuing, Epigallocatechin Gallate's (EGCG) inhibition of protein kinases could shift signaling dynamics to favor SASPase activity, especially in epidermal barrier functions. Sphingosine-1-phosphate (S1P) acts through its receptors to initiate signaling that may culminate in the activation of pathways involving SASPase, like keratinocyte differentiation. Lithium Chloride, by inhibiting GSK-3β, may contribute to β-catenin stabilization, thereby enhancing SASPase-related signaling pathways. Sodium Butyrate, a histone deacetylase inhibitor, could induce hyperacetylation of histones, potentially leading to heightened ASPRV1 gene expression and subsequent SASPase activity. Lysophosphatidic Acid (LPA) mediates responses that could indirectly bolster SASPase activity through keratinocyte proliferation. Quercetin, by inhibiting phosphodiesterases and raising cAMP levels, can enhance PKA activity, which in turn could phosphorylate SASPase. All-trans Retinol, through its metabolism to retinoic acid, augments SASPase activity by supporting keratinocyte differentiation, a process pivotal for SASPase's role in skin health.

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