TFR2 inhibitors are molecules designed to block or modulate the activity of transferrin receptor 2 (TFR2), a membrane protein primarily involved in iron homeostasis. TFR2 is a type II transmembrane receptor that binds to transferrin, a protein responsible for transporting iron in the bloodstream. Unlike its more well-known counterpart, transferrin receptor 1 (TFR1), TFR2 plays a distinct role in regulating iron uptake and sensing iron levels in specific tissues. Inhibitors of TFR2 act by interfering with the receptor's ability to bind transferrin or by preventing the receptor from transmitting signals that regulate iron-related processes. These molecules may achieve inhibition through direct binding to the receptor's extracellular domain or by altering its conformation, thereby disrupting its interaction with transferrin or other associated proteins.
The structural design of TFR2 inhibitors often focuses on targeting key regions of the receptor that are critical for its function, such as the transferrin-binding site or domains involved in receptor dimerization and signaling. By blocking these regions, TFR2 inhibitors can prevent the receptor from functioning normally, which in turn affects downstream molecular pathways that rely on TFR2 activity. These inhibitors can vary in size and chemical composition, ranging from small organic molecules to larger peptides or antibodies. The study of TFR2 inhibitors is important for understanding the broader role of iron regulation at the molecular level, as these compounds help elucidate how TFR2 interacts with other components of the iron transport and sensing machinery. Through this research, the specificity and binding properties of TFR2 inhibitors contribute valuable information to the field of iron metabolism and cellular regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Deferoxamine | 70-51-9 | sc-507390 | 5 mg | $255.00 | ||
As an iron chelator, Deferoxamine may reduce the cellular need for TFR2-mediated iron uptake by decreasing free iron levels. | ||||||
Deferiprone | 30652-11-0 | sc-211220 sc-211220A | 1 g 5 g | $124.00 $134.00 | 5 | |
Deferiprone chelates iron and could lead to lower TFR2 expression by reducing the labile iron pool within cells. | ||||||
Deferasirox | 201530-41-8 | sc-207509 | 2.5 mg | $180.00 | 9 | |
By binding to free iron, Deferasirox could decrease the cellular requirement for TFR2, indirectly inhibiting its activity. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Forskolin increases intracellular cAMP, which could affect iron metabolism and TFR2 expression through various signaling pathways. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Glucocorticoids like Dexamethasone can modulate inflammatory and cellular pathways that may influence TFR2 expression indirectly. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Methotrexate impacts folate metabolism and could indirectly affect TFR2 activity through alterations in cellular proliferation rates. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits mTOR, which is involved in cellular growth and iron metabolism, potentially leading to reduced TFR2 activity. | ||||||
L-Leucine | 61-90-5 | sc-364173 sc-364173A | 25 g 100 g | $21.00 $62.00 | ||
As an activator of mTORC1, Leucine might indirectly modulate TFR2 activity via changes in iron utilization and cellular growth. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $66.00 $325.00 $587.00 $1018.00 | 28 | |
Retinoic Acid can regulate gene expression, potentially affecting the transcriptional level of TFR2. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium affects multiple signaling pathways and could indirectly impact TFR2 expression or iron homeostasis. | ||||||