LT-β inhibitors are a category of chemical compounds designed to impede the biological activity of lymphotoxin-beta (LT-β), a member of the tumor necrosis factor (TNF) superfamily that is integral to the development and organization of lymphoid tissues and the modulation of immune responses. The function of LT-β is largely dependent on its interaction with the LT-β receptor (LTβR), which triggers a series of signaling events influencing various aspects of immune function. LT-β inhibitors can act through several mechanisms to achieve their inhibitory effect. Direct inhibitors may bind to LT-β itself, preventing its interaction with LTβR, thus blocking the initiation of the signaling cascade that would normally follow. Alternatively, they might target the receptor directly, precluding the binding of LT-β.
Indirect inhibitors may work by downregulating the expression of LT-β or LTβR, altering the post-translational modification of the protein, or interfering with the signaling pathways downstream of the receptor that are essential for its biological effects. The exploration of LT-β inhibitors is a scientific endeavor aimed at understanding the intricate pathways of immune system regulation. By employing these inhibitors, researchers can dissect the complex network of signals that govern immune response and lymphoid architecture, shedding light on fundamental processes that underlie immune system development and function. The insights gained from such research can provide a deeper understanding of the immune system's mechanisms, potentially unveiling new avenues for modulating immune responses in various contexts.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Montelukast Sodium | 151767-02-1 | sc-202231 sc-202231A sc-202231B | 10 mg 25 mg 250 mg | $51.00 $85.00 $161.00 | 5 | |
Montelukast is a selective inhibitor of the LTB receptor, specifically targeting the LTB4 receptor. | ||||||
Zileuton | 111406-87-2 | sc-204417 sc-204417A sc-204417B sc-204417C | 10 mg 50 mg 1 g 75 g | $84.00 $307.00 $369.00 $1254.00 | 8 | |
Zileuton is an inhibitor of 5-lipoxygenase (5-LO), an enzyme involved in the synthesis of leukotrienes. By inhibiting 5-LO, zileuton reduces the production of leukotrienes, including LTB4. | ||||||
SC 57461A | 423169-68-0 | sc-204266 sc-204266A | 5 mg 25 mg | $151.00 $577.00 | 1 | |
SC-57461A is a selective inhibitor of LTA4 hydrolase, an enzyme involved in the metabolism of LTBBy inhibiting LTA4 hydrolase, SC-57461A reduces the levels of LTB4, thereby attenuating the inflammatory response. | ||||||
MK-571 | 115103-85-0 | sc-201340 sc-201340A | 5 mg 25 mg | $109.00 $421.00 | 8 | |
MK-571 is an inhibitor of the multidrug resistance-associated protein 1 (MRP1), which is involved in the transport of leukotrienes. By inhibiting MRP1, MK-571 decreases the efflux of leukotrienes from cells and reduces their pro-inflammatory effects. | ||||||
Pranlukast hemihydrate | 150821-03-7 | sc-215745 | 5 mg | $73.00 | ||
Pranlukast is another LTB receptor antagonist that competitively inhibits LTB4 binding to its receptor. | ||||||
LY293111 | 161172-51-6 | sc-221866 sc-221866A | 500 µg 1 mg | $141.00 $347.00 | ||
LY293111 is a selective LTB4 receptor antagonist that competitively binds to and inhibits LTB4 receptor activation. It has shown efficacy in animal models of inflammatory diseases. | ||||||