Interleukin-17C (IL-17C) is a member of the IL-17 family, a unique cohort of cytokines implicated in the regulation of inflammatory responses and the orchestration of autoimmunity. Unlike its more studied counterparts, IL-17C exerts its effects primarily on epithelial cells, playing a crucial role in mucosal immunity and the body's defense against extracellular pathogens. It achieves this by promoting the expression of antimicrobial peptides, chemokines, and cytokines that facilitate the recruitment and activation of neutrophils and other immune cells to sites of infection. IL-17C's function is tightly linked to the maintenance of epithelial barrier integrity and the regulation of tissue repair processes. Its activity is modulated through its interaction with a distinct receptor complex, composed of the IL-17 receptor E (IL-17RE) and IL-17RA, highlighting a sophisticated mechanism of action that diverges from traditional cytokine-receptor engagements.
The inhibition of IL-17C involves targeting either the cytokine itself, its receptor complex, or the downstream signaling pathways it activates. This can be achieved through various biological mechanisms that directly or indirectly reduce the biological activity of IL-17C. One common method of inhibition includes the use of neutralizing antibodies that bind to IL-17C, preventing its interaction with the IL-17RE/RA receptor complex, thereby blocking its pro-inflammatory signaling cascade. Another approach targets the receptor complex itself, disrupting the IL-17C-mediated signaling pathway. Additionally, small molecule inhibitors can interfere with the intracellular signaling pathways activated by IL-17C, such as those involving NF-κB and MAPKs, which are critical for the transcription of target genes involved in inflammation and immune responses. These inhibitory mechanisms collectively contribute to the reduction of IL-17C-mediated effects on epithelial cells, potentially attenuating excessive inflammatory responses without directly naming specific inhibitors, focusing instead on the broad strategies employed to mitigate the cytokine's activity within the immune system.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Apremilast | 608141-41-9 | sc-480062 | 5 mg | $444.00 | ||
Apremilast inhibits phosphodiesterase 4 (PDE4), which can lead to a reduction in pro-inflammatory cytokines and thus can downregulate IL-17C signaling indirectly. | ||||||
Ruxolitinib | 941678-49-5 | sc-364729 sc-364729A sc-364729A-CW | 5 mg 25 mg 25 mg | $251.00 $500.00 $547.00 | 16 | |
Ruxolitinib is also a JAK inhibitor with a similar mechanism to Tofacitinib, thus it can modulate the signaling pathways that IL-17C is part of. | ||||||
Cyclosporin A | 59865-13-3 | sc-3503 sc-3503-CW sc-3503A sc-3503B sc-3503C sc-3503D | 100 mg 100 mg 500 mg 10 g 25 g 100 g | $63.00 $92.00 $250.00 $485.00 $1035.00 $2141.00 | 69 | |
Cyclosporin A inhibits calcineurin, which ultimately leads to a decrease in T-cell activation and can have an effect on cytokine production, including IL-17C. | ||||||
Sulfasalazine | 599-79-1 | sc-204312 sc-204312A sc-204312B sc-204312C | 1 g 2.5 g 5 g 10 g | $61.00 $77.00 $128.00 $209.00 | 8 | |
Sulfasalazine can inhibit NF-κB, which is a transcription factor that can regulate the expression of IL-17C. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Methotrexate can inhibit dihydrofolate reductase and has immunosuppressive properties that can lead to a reduction in cytokine production, possibly affecting IL-17C. | ||||||
BMS 582949 | 623152-17-0 | sc-507348 | 5 mg | $510.00 | ||
BMS-582949 is a p38 MAPK inhibitor, this kinase is involved in the production of pro-inflammatory cytokines and can modulate IL-17C signaling. | ||||||
NFκB Activation Inhibitor II, JSH-23 | 749886-87-1 | sc-222061 sc-222061C sc-222061A sc-222061B | 5 mg 10 mg 50 mg 100 mg | $214.00 $257.00 $1775.00 $2003.00 | 34 | |
JSH-23 is an NF-κB inhibitor, which can prevent the nuclear translocation of NF-κB and may decrease the expression of IL-17C. | ||||||