CD16-2 inhibitors belong to a specialized chemical class of compounds designed to target and modulate the CD16-2 receptor, also known as FcγRIIIb. CD16-2 is a cell surface receptor primarily found on immune cells such as neutrophils, monocytes, and macrophages. Its role is central to the immune response as it is involved in the recognition and binding of immunoglobulin G (IgG) antibodies, particularly during immune complex formation and antibody-dependent cellular cytotoxicity (ADCC). CD16-2 receptors play a crucial role in fine-tuning the immune response by mediating the activation and recruitment of immune cells to sites of infection or tissue damage. Inhibitors of CD16-2 are designed to modulate this receptor's activity, which can have significant implications for immune responses and various immunological processes.
CD16-2 inhibitors are characterized by their ability to interfere with the binding of IgG antibodies to CD16-2 receptors, ultimately inhibiting downstream signaling cascades and cellular responses. These inhibitors can function through various mechanisms, including competitive binding to CD16-2, blocking its engagement with IgG antibodies, or altering the conformation of the receptor to prevent effective antibody recognition. By doing so, CD16-2 inhibitors have the ability to inhibit immune cell activation, migration, and phagocytosis, which can have broad implications in the context of immunology and host defense mechanisms.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib is a tyrosine kinase inhibitor that can inhibit the Src family kinases, which are downstream of CD16 signaling, possibly reducing ADCC. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
PP2 is another Src family kinase inhibitor, which can suppress the activation of kinases that are important for the signaling cascade following CD16 engagement. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a PI3K inhibitor, which can suppress the PI3K-Akt pathway, a key pathway in the signaling of CD16 that leads to cellular responses. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is also a PI3K inhibitor, it can inhibit the kinase activity of PI3K, likely diminishing the signal transduction from CD16. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is another MEK inhibitor, which can prevent the activation of the MAPK/ERK pathway downstream of CD16. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a p38 MAPK inhibitor which can impede the p38 MAPK pathway, potentially diminishing the inflammatory response mediated by CD16. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is a JNK inhibitor that can affect the JNK signaling cascade, which may be involved in CD16-mediated cellular processes. | ||||||
BAY 11-7082 | 19542-67-7 | sc-200615B sc-200615 sc-200615A | 5 mg 10 mg 50 mg | $61.00 $83.00 $349.00 | 155 | |
BAY 11-7082 is an NF-κB inhibitor that can reduce the transcription of NF-κB target genes, which could be upregulated following CD16 signaling. | ||||||
IKK 16 | 1186195-62-9 | sc-204009 sc-204009A | 10 mg 50 mg | $219.00 $924.00 | 2 | |
IKK-16 is an inhibitor of IKK, which can prevent the activation of NF-κB, a transcription factor that can be activated by CD16. | ||||||
Caffeic acid phenethyl ester | 104594-70-9 | sc-200800 sc-200800A sc-200800B | 20 mg 100 mg 1 g | $70.00 $290.00 $600.00 | 19 | |
CAPE is an NF-κB inhibitor, which can suppress the activation of NF-κB, potentially affecting the gene expression alterations following CD16 engagement. | ||||||