Klra22 inhibitors represent a chemical class targeting the Klra22 gene, which is part of the killer cell lectin-like receptor family A (KLRA) found in mammals. KLRA receptors are crucial components of immune regulation, particularly in modulating the activity of natural killer (NK) cells. These inhibitors function by specifically binding to the Klra22 receptor or its associated signaling components, thereby modulating or blocking its natural activity. By inhibiting Klra22, these compounds can alter downstream signaling pathways that influence cellular processes like immune recognition, cytokine production, and cytotoxic responses. The specific binding affinities and mechanistic actions of these inhibitors are often determined by their molecular structures, which allow them to interact precisely with the Klra22 receptor or its ligand-binding domains.
Structurally, Klra22 inhibitors are designed with functional groups that enhance their ability to bind effectively to the Klra22 receptor. These molecules often feature core chemical scaffolds that allow for high specificity in binding and inhibit potential off-target effects. This binding specificity is vital for minimizing unintended interactions with other members of the KLRA family, which could lead to widespread immune dysregulation. The precise molecular designs of Klra22 inhibitors are informed by studies of the receptor's 3D structure, helping researchers to develop compounds that fit into the receptor's binding site with high affinity. This specificity in chemical interactions ensures that the Klra22 inhibitors effectively modulate immune signaling pathways associated with this receptor, making them valuable tools in immunological studies.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 | $62.00 $90.00 $299.00 $475.00 $1015.00 $2099.00 | 69 | |
An immunosuppressant that can indirectly affect NKG2D signaling by altering T-cell responses. | ||||||
FK-506 | 104987-11-3 | sc-24649 sc-24649A | 5 mg 10 mg | $76.00 $148.00 | 9 | |
Inhibits calcineurin, leading to reduced T-cell activation and potentially modulating NKG2D-mediated functions. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Inhibits mTOR, affecting T-cell proliferation and potentially NKG2D signaling pathways. | ||||||
Mycophenolate mofetil | 128794-94-5 | sc-200971 sc-200971A | 20 mg 100 mg | $36.00 $107.00 | 1 | |
Inhibits inosine monophosphate dehydrogenase, suppressing proliferation of T and B cells, which could indirectly impact NKG2D signaling. | ||||||
Prednisolone | 50-24-8 | sc-205815 sc-205815A | 1 g 5 g | $82.00 $248.00 | 2 | |
Suppress inflammation and immune responses, potentially affecting NKG2D-mediated cytotoxic activity. | ||||||
Azathioprine | 446-86-6 | sc-210853D sc-210853 sc-210853A sc-210853B sc-210853C | 500 mg 1 g 2 g 5 g 10 g | $199.00 $173.00 $342.00 $495.00 $690.00 | 1 | |
A purine analog that inhibits lymphocyte proliferation, potentially modulating NKG2D signaling indirectly. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $92.00 $209.00 | 33 | |
An anti-inflammatory drug that inhibits dihydrofolate reductase, affecting immune cell proliferation and potentially NKG2D signaling. | ||||||
Leflunomide | 75706-12-6 | sc-202209 sc-202209A | 10 mg 50 mg | $20.00 $81.00 | 5 | |
Inhibits dihydroorotate dehydrogenase, affecting pyrimidine synthesis and T-cell proliferation, with potential indirect effects on NKG2D. | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $109.00 $350.00 | 8 | |
Modulates the immune response and has anti-inflammatory properties, which could indirectly influence NKG2D activity. | ||||||
Lenalidomide | 191732-72-6 | sc-218656 sc-218656A sc-218656B | 10 mg 100 mg 1 g | $49.00 $367.00 $2030.00 | 18 | |
An immunomodulatory drug that can affect T-cell and NK-cell function, potentially modulating NKG2D signaling. | ||||||