MHC inhibitors are a class of chemical compounds that interact with the Major Histocompatibility Complex (MHC), a group of proteins essential for antigen presentation and immune recognition. The MHC molecules are divided into two major classes: MHC class I, which is responsible for presenting intracellular antigens to CD8+ T cells, and MHC class II, which presents extracellular antigens to CD4+ T cells. Inhibitors of MHC function typically work by blocking the formation of the MHC-peptide complex or by interfering with the stability of this complex on the cell surface. By inhibiting these functions, MHC inhibitors can disrupt antigen processing and presentation, thereby altering the cellular signaling processes involved in immune recognition. These interactions can lead to changes in the recruitment and activation of T cells, which are central to immune response regulation.
MHC inhibitors often target specific binding sites on the MHC molecule or associated accessory proteins, such as β2-microglobulin in MHC class I or invariant chains in MHC class II, to inhibit their function. In addition, some MHC inhibitors may prevent the trafficking of MHC molecules to the cell surface, while others may destabilize the MHC-peptide complex, leading to its rapid degradation. The chemical structures of MHC inhibitors are diverse, ranging from small organic molecules to more complex peptides and synthetic derivatives. These inhibitors are highly specific to the MHC subtypes they target and are often designed to exploit the unique structural features of MHC molecules. Their ability to modulate immune signaling pathways at a fundamental level has made them a focus of interest in various scientific studies, particularly for understanding immune response mechanisms.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
A77 1726 | 163451-81-8 | sc-207235 | 10 mg | $80.00 | 14 | |
A771726 is a selective inhibitor of dihydroorotate dehydrogenase (DHODH), an enzyme involved in pyrimidine biosynthesis, leading to MHC inhibition. | ||||||
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 suppresses T cell activation and subsequent MHC expression. | ||||||
FK-506 | 104987-11-3 | sc-24649 sc-24649A | 5 mg 10 mg | $78.00 $151.00 | 9 | |
FK506 binds to FK506-binding protein 12 (FKBP12), resulting in inhibition of calcineurin and downregulation of MHC expression. | ||||||
Mycophenolate mofetil | 128794-94-5 | sc-200971 sc-200971A | 20 mg 100 mg | $37.00 $109.00 | 1 | |
Mycophenolate mofetil inhibits inosine monophosphate dehydrogenase (IMPDH), ultimately leading to decreased MHC expression. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits the mTOR pathway, which negatively regulates MHC expression and antigen presentation. | ||||||
Auranofin | 34031-32-8 | sc-202476 sc-202476A sc-202476B | 25 mg 100 mg 2 g | $153.00 $214.00 $4000.00 | 39 | |
Auranofin inhibits thioredoxin reductase, leading to decreased MHC expression through modulation of redox signaling. | ||||||
Leflunomide | 75706-12-6 | sc-202209 sc-202209A | 10 mg 50 mg | $20.00 $83.00 | 5 | |
Leflunomide inhibits dihydroorotate dehydrogenase (DHODH), an enzyme involved in pyrimidine biosynthesis, leading to MHC downregulation. | ||||||
Azathioprine | 446-86-6 | sc-210853D sc-210853 sc-210853A sc-210853B sc-210853C | 500 mg 1 g 2 g 5 g 10 g | $203.00 $176.00 $349.00 $505.00 $704.00 | 1 | |
Azathioprine inhibits purine synthesis, ultimately leading to decreased MHC expression. | ||||||