The chemical class known as IL-28R Activators comprises a diverse array of compounds that function to initiate or enhance the activation of the Interleukin-28 Receptor (IL-28R). IL-28R, integral to immune signaling, primarily interacts with cytokines like IL-28A, IL-28B, and IL-29. These interactions play a crucial role in mediating antiviral responses, particularly in epithelial tissues. IL-28R activators are not a homogenous group; they encompass various chemical structures and origins, ranging from synthetic molecules to naturally occurring substances. These activators work either by directly engaging with the receptor or indirectly through pathways that lead to its activation. The direct activators mimic the action of natural ligands, binding to IL-28R and triggering a series of intracellular signaling cascades, predominantly the JAK-STAT pathway. This leads to the transcriptional activation of genes involved in antiviral defenses. On the other hand, indirect activators influence upstream signaling mechanisms or modulate the cellular environment in a manner that promotes IL-28R activation, even though they do not interact with the receptor directly.
Understanding the action of IL-28R activators requires delving into the complexities of immune signaling and the body's antiviral defenses. Upon activation, IL-28R orchestrates a response that is crucial for inhibiting viral replication and spread. The unique aspect of these activators lies in their ability to manipulate this specific aspect of the immune response, making them of interest in the study of antiviral mechanisms. Their relevance extends beyond simple receptor activation; they represent a crucial tool in unraveling the sophisticated network of immune signaling. By stimulating IL-28R, these compounds provide insight into how the body's innate defenses are mobilized against viral intruders. This is especially significant in understanding the nuanced interplay between different cytokines and receptors in immune regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
R-848 | 144875-48-9 | sc-203231 sc-203231A sc-203231B sc-203231C | 5 mg 25 mg 100 mg 500 mg | $102.00 $306.00 $510.00 $1559.00 | 12 | |
R-848 (Resiquimod) can act as an immune response modifier. Its impact on viral and interferon-related pathways may influence IL-28R. | ||||||
Imiquimod | 99011-02-6 | sc-200385 sc-200385A | 100 mg 500 mg | $67.00 $284.00 | 6 | |
Imiquimod, known to modulate immune responses, may have indirect effects on IL-28R expression through its action on related pathways. | ||||||
Gardiquimod | 1020412-43-4 | sc-221663 sc-221663A sc-221663B sc-221663C sc-221663D sc-221663E sc-221663F | 25 mg 50 mg 100 mg 250 mg 5 g 10 g 25 g | $157.00 $282.00 $516.00 $1177.00 $20138.00 $32779.00 $70753.00 | 1 | |
As an agonist for Toll-like receptors, Gardiquimod may play a role in the potential upregulation of IL-28R during immune responses. | ||||||
Rosmarinic Acid | 20283-92-5 | sc-202796 sc-202796A | 10 mg 50 mg | $58.00 $109.00 | 4 | |
Some studies suggest that rosmarinic acid may affect interferon-related pathways, potentially influencing IL-28R expression. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin is known to modulate immune responses and may affect IL-28R expression indirectly. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
As a tyrosine kinase inhibitor, Genistein can affect various signaling pathways, potentially influencing IL-28R. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Curcumin can modulate several immune and cellular pathways, which might have indirect effects on IL-28R expression. | ||||||