SOX15 Activators are a diverse set of chemical compounds that facilitate the functional activity of SOX15 through various biochemical activation mechanisms. Retinoic Acid, for instance, promotes cell differentiation by interacting with the retinoic acid receptor pathway, which could induce the upregulation of SOX15, enhancing its role in developmental processes. Similarly, the cAMP analog Dibutyryl-cAMP and Forskolin both raise intracellular cAMP levels, leading to PKA activation which may trigger a cascade of transcriptional events increasing the activity of SOX15. PMA, through the activation of PKC, may also modulate transcriptional networks that indirectly upregulate SOX15's function. Further influencing the epigenetic landscape, Trichostatin A, as a histone deacetylase inhibitor, and 5-Azacytidine, as a DNA methyltransferase inhibitor, both contribute to a more transcriptionally active chromatin state that may favor SOX15 expression and its subsequent activity in gene regulation. Sodium Butyrate, another HDAC inhibitor, complements this epigenetic modulation, potentially enhancing SOX15's role in cellular differentiation.
Epigallocatechin Gallate (EGCG) and Resveratrol both exert effects on signaling pathways that can indirectly lead to an increase in SOX15 activity, although their exact mechanisms may vary. EGCG might impact transcriptional machinery or epigenetic modifications associated with SOX15, while Resveratrol, by activating sirtuin pathways, might enhance SOX15 activity through alterations in gene expression profiles linked to SOX15's functions. Lithium Chloride, through inhibition of GSK-3 and subsequent activation of β-catenin, might stimulate the transcription of Wnt target genes, potentially including SOX15, thereby augmenting its developmental functions. Valproic Acid, by inhibiting HDAC, could also lead to increased SOX15 expression and activity. Lastly, Biochanin A, acting as a weak estrogen receptor agonist, may influence the transcription of estrogen-responsive genes, potentially including SOX15, and thereby enhance its activity in gene regulation. Collectively, these SOX15 Activators, through their targeted effects on cellular signaling and gene expression, facilitate the enhancement of SOX15-mediated functions without the need for upregulating its expression through direct activation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid influences cell differentiation through the retinoic acid receptor (RAR) pathway. Activation of RAR can lead to the upregulation of downstream target genes, including SOX15, enhancing SOX15's role in cell differentiation and development. | ||||||
Dibutyryl-cAMP | 16980-89-5 | sc-201567 sc-201567A sc-201567B sc-201567C | 20 mg 100 mg 500 mg 10 g | $45.00 $130.00 $480.00 $4450.00 | 74 | |
Dibutyryl-cAMP acts as a cell-permeable analog of cyclic AMP (cAMP), activating PKA. PKA phosphorylation can lead to the activation of transcription factors, which may include SOX15, thereby potentially increasing its activity in the regulation of gene expression. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin stimulates adenylate cyclase, increasing intracellular cAMP levels and thereby activating PKA. PKA activation can enhance the activity of various transcription factors, possibly including SOX15, in processes like cell differentiation. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA activates protein kinase C (PKC), which can influence numerous signaling pathways. PKC activation may enhance SOX15 activity indirectly by modulating related transcriptional networks that SOX15 is part of. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is a histone deacetylase inhibitor, which leads to a more relaxed chromatin structure and potentially increased transcription of certain genes, including SOX15, thus enhancing its functional activity. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine is a DNA methyltransferase inhibitor that can lead to the demethylation of gene promoters, including potentially that of SOX15, resulting in enhanced gene expression and protein activity. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium Butyrate acts as a histone deacetylase inhibitor, leading to increased acetylation of histones and a more open chromatin state, which may upregulate SOX15 expression and activity. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
EGCG is a polyphenol that can modulate various signaling pathways, potentially including those that regulate gene expression. EGCG might enhance SOX15 activity indirectly by influencing the transcriptional machinery or epigenetic marks associated with SOX15. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol activates sirtuin pathways, which are involved in gene silencing and longevity. Activation of these pathways could potentially enhance the activity of SOX15 indirectly by affecting gene expression profiles linked to SOX15 function. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium Chloride inhibits GSK-3, leading to stabilization and activation of β-catenin. This may result in the transcriptional activation of Wnt target genes, which could include SOX15, enhancing its activity in cell differentiation and developmental processes. | ||||||