Follicular Dendritic Cell (FDC) Marker Inhibitors are a specialized class of chemical compounds that target specific markers expressed on the surface of follicular dendritic cells. FDCs are unique stromal cells located within the germinal centers of lymphoid follicles and play a pivotal role in the immune system by facilitating B-cell maturation and antigen presentation. These inhibitors function by binding to FDC-specific markers such as complement receptors (e.g., CD21, CD35) or Fc receptors, thereby modulating the interactions between FDCs and B cells. By inhibiting these markers, the compounds can affect the retention and presentation of immune complexes, influence germinal center reactions, and alter signaling pathways critical for immune responses.
Chemically, Follicular DC Marker Inhibitors encompass a diverse array of molecules, including small organic compounds, peptides, and monoclonal antibodies. The design of these inhibitors often involves high-throughput screening and structure-based drug design to identify compounds with high affinity and specificity for FDC markers. Small molecule inhibitors may feature functional groups that facilitate strong interactions with target proteins through hydrogen bonding, hydrophobic interactions, or ionic bonds. Peptide-based inhibitors mimic natural ligands or binding domains, providing specificity and reduced off-target effects. Monoclonal antibodies are designed to bind precisely to epitopes on FDC markers, offering high specificity. Advanced techniques such as X-ray crystallography and molecular docking simulations aid in understanding the binding mechanisms and optimizing the chemical structures for enhanced efficacy. Research into these inhibitors contributes to a deeper understanding of FDC functions and the molecular mechanisms underlying immune system regulation.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine may disrupt endosomal acidification and impede autophagic processes, leading to a buildup of cellular debris and a subsequent decrease in FDC marker expression due to impaired protein turnover. | ||||||
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 | |
By inhibiting calcineurin, Cyclosporin A could prevent the dephosphorylation and translocation of NFAT transcription factors to the nucleus, thereby decreasing transcription of genes encoding FDC markers. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine could induce DNA demethylation, which may silence gene promoters essential for the synthesis of FDC markers, leading to their reduced expression on the cell surface. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $92.00 $209.00 | 33 | |
Methotrexate's inhibition of dihydrofolate reductase compromises thymidylate synthesis, potentially leading to DNA synthesis interruption and subsequent downregulation of FDC marker gene expression. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid could recalibrate gene transcription by activating retinoid receptors, resulting in the reduced transcription of FDC marker genes and a lower presence of these markers on the cell surface. | ||||||
hydroxychloroquine | 118-42-3 | sc-507426 | 5 g | $56.00 | 1 | |
Hydroxychloroquine may interfere with glycosylation processes necessary for proper FDC marker folding and stability, leading to a decrease in their expression. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol could inhibit the transcriptional activity of NF-κB, potentially leading to a decrease in the expression of genes responsible for the synthesis of FDC markers. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin's suppression of the NF-κB pathway may lead to a reduction in the transcription of FDC marker genes, thereby decreasing their surface expression. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $26.00 $92.00 $120.00 $310.00 $500.00 $908.00 $1821.00 | 46 | |
By inhibiting tyrosine kinases, Genistein could disrupt intracellular signaling required for the expression of FDC markers, resulting in their diminished presence. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $150.00 $286.00 $479.00 $1299.00 $8299.00 $915.00 | 22 | |
DL-Sulforaphane is known to inhibit histone deacetylase, which could lead to changes in chromatin structure and a consequent decrease in the expression of FDC marker genes. |