HCC-4 inhibitors are a class of chemical compounds designed to specifically target and modulate the activity of HCC-4, also known as CCL16, a chemokine primarily involved in immunological signaling and cellular communication. Chemokines like HCC-4 are small, structurally related cytokines that mediate various biological processes, such as cell migration, immune responses, and inflammatory pathways. HCC-4 inhibitors act by binding to the chemokine or its receptors, which subsequently disrupts the signaling cascades driven by HCC-4. These inhibitors can be either small molecules, peptides, or antibodies engineered to fit into the binding domains of HCC-4 or its associated receptors, effectively preventing its interaction with other cellular components.
From a biochemical perspective, the specificity of HCC-4 inhibitors often depends on their ability to recognize distinct molecular features of the chemokine, such as its conformation, binding motifs, or post-translational modifications. The chemical structures of these inhibitors are typically optimized to ensure that they maintain high binding affinity while avoiding off-target interactions that could impact other chemokines or proteins. Researchers are particularly interested in the design and synthesis of these inhibitors, as they provide tools to dissect the biological roles of HCC-4 in various cellular contexts. These compounds are often characterized through biochemical assays, structural analysis, and receptor-binding studies to better understand how they interact with HCC-4 and regulate its function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
SB 225002 | 182498-32-4 | sc-202803 sc-202803A | 1 mg 5 mg | $35.00 $100.00 | 2 | |
This CXCR2 inhibitor blocks the CXCR2 receptor, where HCC-4 serves as a ligand, effectively attenuating its signaling. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
Inhibits PI3K, a downstream mediator of HCC-4. This impacts HCC-4-induced chemotaxis and immune cell migration. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
This MEK inhibitor interferes with the MAPK pathway. HCC-4 can activate MAPK via G-protein-coupled receptors, thus its action is modulated. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
This mTOR inhibitor impacts a pathway that can be activated by HCC-4, thus indirectly reducing its capability to mediate cell migration. | ||||||
BAPTA/AM | 126150-97-8 | sc-202488 sc-202488A | 25 mg 100 mg | $138.00 $449.00 | 61 | |
Calcium chelator affecting calcium-dependent pathways activated by HCC-4, thus decreasing its capability to activate immune cells. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Protein kinase inhibitor that targets multiple kinases involved in HCC-4 signaling, thereby modulating its activity. | ||||||
Calphostin C | 121263-19-2 | sc-3545 sc-3545A | 100 µg 1 mg | $336.00 $1642.00 | 20 | |
PKC inhibitor affecting the pathway where HCC-4 acts as a signaling molecule, inhibiting its cellular effects. | ||||||
Ro 31-8220 | 138489-18-6 | sc-200619 sc-200619A | 1 mg 5 mg | $90.00 $240.00 | 17 | |
Another PKC inhibitor, affecting the same pathways as Calphostin C, thus reducing HCC-4’s ability to activate immune cells. | ||||||