GITRL inhibitors, short for Glucocorticoid-Induced Tumor Necrosis Factor Ligand inhibitors, belong to a class of chemical compounds that primarily target a specific molecular pathway within the immune system. These inhibitors are designed to modulate the activity of GITRL, a protein belonging to the tumor necrosis factor (TNF) superfamily. GITRL, or Glucocorticoid-Induced Tumor Necrosis Factor Ligand, is a cell surface protein that plays a pivotal role in regulating immune responses. It is primarily expressed on antigen-presenting cells, such as dendritic cells and macrophages, and interacts with its receptor, GITR (Glucocorticoid-Induced Tumor Necrosis Factor Receptor), which is found on various immune cells, including T cells.
The main function of GITRL and its corresponding receptor GITR is to modulate the activation and differentiation of T cells. When GITRL binds to GITR, it can either stimulate or suppress T cell responses depending on the context of the immune response. In certain situations, such as during chronic inflammation or autoimmune diseases, overactivation of this pathway can lead to excessive immune responses and tissue damage. GITRL inhibitors, therefore, are developed to block or regulate the GITRL-GITR interaction, thereby modulating T cell activation and immune responses. These inhibitors can be important tools in research and drug development aimed at understanding and potentially controlling immune-related disorders and diseases.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Tyrosine kinase inhibitor targeting BCR-ABL fusion protein. | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $63.00 $114.00 $218.00 $349.00 | 74 | |
Inhibits epidermal growth factor receptor (EGFR) signaling, employed in non-small cell lung cancer research. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Multi-kinase inhibitor affecting RAF/MEK/ERK pathway, used in hepatocellular carcinoma and renal cell carcinoma. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Proteasome inhibitor disrupting protein degradation in multiple myeloma and mantle cell lymphoma. | ||||||
MDV3100 | 915087-33-1 | sc-364354 sc-364354A | 5 mg 50 mg | $245.00 $1051.00 | 7 | |
Antagonizes androgen receptor signaling, applied in prostate cancer research. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $131.00 $651.00 | 7 | |
mTOR inhibitor suppressing cell growth. | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $87.00 $135.00 $293.00 $505.00 $3827.00 | 42 | |
Targets EGFR tyrosine kinase, inhibiting cell proliferation, employed in non-small cell lung cancer research. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
Tyrosine kinase inhibitor targeting BCR-ABL and SRC kinases. | ||||||
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $114.00 $166.00 $947.00 | 19 | |
Selectively inhibits MEK1/2, blocking cell proliferation in BRAF-mutant melanoma and other cancers. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $156.00 | 5 | |
Irreversible BTK inhibitor, suppressing B-cell signaling in chronic lymphocytic leukemia and lymphoma. | ||||||