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.
Items 1 to 10 of 15 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
By inducing DNA hypomethylation, 5-Azacytidine could decrease CD8β expression through the reactivation of silenced genes that compete or interfere with the transcriptional machinery of the CD8β gene. | ||||||
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 | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
Trichostatin A could downregulate CD8β by inhibiting histone deacetylases, leading to hyperacetylation of histones, thereby condensing the chromatin at the CD8β gene locus and suppressing its transcription. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium butyrate may downregulate CD8β expression by inhibiting histone deacetylases, which would alter the acetylation status of histones associated with the CD8β gene and decrease its transcriptional activity. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $87.00 | 9 | |
Valproic Acid is another histone deacetylase inhibitor that can impact gene expression and possibly reduce the levels of CD8-β. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Bortezomib might reduce CD8β expression by inhibiting the proteasome, leading to the accumulation of misfolded proteins, which can activate cellular stress responses that attenuate CD8β gene transcription. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin is an mTOR inhibitor, which can lead to altered protein synthesis and potentially reduce the expression of CD8-β. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY 294002 might reduce CD8β expression by inhibiting PI3K, leading to a reduction in AKT signaling and subsequent downregulation of NF-κB, which is essential for the transcriptional activation of the CD8β gene. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Wortmannin is another PI3K inhibitor that can interfere with cellular signaling and possibly diminish CD8-β levels. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB 203580 could inhibit p38 MAPK and thereby decrease CD8β expression by reducing the activation of AP-1, a transcription factor required for CD8β gene transcription. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
By inhibiting JNK signaling, SP600125 could downregulate CD8β by preventing the phosphorylation of transcription factors that are necessary for the initiation of CD8β gene transcription. | ||||||