GROβ inhibitors are a category of chemical agents designed to selectively interfere with the biological activity of the chemokine known as Growth-regulated oncogene-beta (GROβ), also referred to as CXCL2. GROβ is a small cytokine belonging to the CXC chemokine family that is involved in a variety of cellular processes, including the regulation of movement and activation of cells, particularly those related to the immune system. Inhibitors of GROβ function by binding to the chemokine itself or by interacting with its receptor, CXCR2, thereby impeding its interaction with target cells. The inhibition can occur through various mechanisms, such as blocking the receptor-binding site on the chemokine, altering the conformation of the chemokine or receptor, or competing with the chemokine for receptor binding. The specificity and selectivity of these inhibitors are critical, as they must discriminate between GROβ and other closely related chemokines within the CXC family to ensure precise modulation of its activity.
The chemical structures of GROβ inhibitors are diverse, reflecting the complexity of targeting a specific protein-protein interaction. These molecules may be small organic compounds, peptides, peptidomimetics, or even larger biological molecules such as antibodies or engineered protein fragments. The design of these inhibitors often involves a detailed understanding of the molecular architecture of GROβ and its receptor, which can be found in techniques like X-ray crystallography or NMR spectroscopy. By mapping the interaction surfaces between GROβ and CXCR2, researchers can identify key amino acid residues and structural features that are critical for their interaction. GROβ inhibitors are then crafted to target these areas to achieve effective inhibition.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Targets mTOR, inhibiting cell growth and proliferation by disrupting the PI3K/Akt/mTOR pathway. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $138.00 $380.00 | 101 | |
Forms DNA cross-links, preventing DNA replication and transcription, leading to cell death. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $272.00 | 18 | |
Blocks estrogen receptors, used for breast cancer by inhibiting estrogen signaling. | ||||||
Lovastatin | 75330-75-5 | sc-200850 sc-200850A sc-200850B | 5 mg 25 mg 100 mg | $29.00 $90.00 $339.00 | 12 | |
Inhibits HMG-CoA reductase, reducing cholesterol synthesis and lowering LDL cholesterol levels. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor that reduces stomach acid production by irreversibly inhibiting H+/K+ ATPase. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Inhibits multiple kinases including RAF and VEGFR, used to target angiogenesis and cell proliferation in cancer. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Blocks proteasome activity, preventing protein degradation, and inducing apoptosis in cancer cells. | ||||||
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 | |
Targets the epidermal growth factor receptor (EGFR), hindering signaling pathways in cancer cells. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Inhibits xanthine oxidase, decreasing uric acid production and used to manage gout and hyperuricemia. | ||||||