CD8β inhibitors are chemical compounds designed to specifically target the CD8β protein, which forms part of the CD8 receptor complex found on the surface of cytotoxic T cells. The CD8 receptor exists either as a homodimer of CD8α (CD8αα) or as a heterodimer consisting of CD8α and CD8β (CD8αβ). CD8β is essential for enhancing the binding affinity of the CD8 receptor to major histocompatibility complex class I (MHC I) molecules on the surface of target cells, particularly during antigen presentation. The interaction between the CD8 receptor and MHC I stabilizes the engagement between cytotoxic T cells and cells that present antigens, such as virus-infected or abnormal cells. Inhibitors of CD8β aim to disrupt this interaction, potentially altering the downstream signaling pathways and processes involved in immune recognition and response.
The development of CD8β inhibitors focuses on designing molecules that bind specifically to the CD8β chain, blocking its interaction with MHC I molecules. These inhibitors could be small molecules, peptides, or biologic agents that are structurally engineered to target the CD8β domain with high specificity. A key aspect of designing CD8β inhibitors involves ensuring that the inhibitors can distinguish between CD8β and other similar proteins, including the CD8α chain, to avoid off-target effects. Additionally, the inhibitors must possess suitable chemical properties, such as solubility, stability, and binding affinity, to effectively inhibit the function of CD8β in relevant biological environments. By blocking CD8β, these compounds provide valuable tools for investigating the precise role of CD8β in T cell activation, immune cell communication, and antigen recognition, shedding light on how this receptor contributes to the immune response at the molecular level.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
Resveratrol could inhibit CD8β expression by activating sirtuins, which in turn may deacetylate histones at the CD8β gene locus, leading to chromatin compaction and reduced transcriptional activity. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD 98059 may inhibit MEK, which in turn could decrease CD8β expression by preventing the activation of ERK, a kinase necessary for the phosphorylation of transcription factors that promote CD8β gene transcription. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Dexamethasone is able to decrease CD8β expression by activating glucocorticoid receptors, which may translocate to the nucleus and repress transcriptional activation of the CD8β gene by antagonizing the activity of AP-1. | ||||||
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 may decrease CD8β expression by inhibiting the activation of NF-κB and AP-1, transcription factors that are involved in the transcriptional activation of the CD8β gene. | ||||||
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 could decrease the expression of CD8β by inhibiting phosphorylation of STATs and preventing their dimerization, which is necessary for the transcriptional activation of the CD8β gene. | ||||||