Hrs (Hepatocyte growth factor-regulated tyrosine kinase substrate) inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the Hrs protein. Hrs is a key player in the regulation of intracellular protein trafficking and endocytic processes within cells. It plays a critical role in the endosomal sorting and recycling of cell surface receptors, including receptor tyrosine kinases (RTKs) and G protein-coupled receptors (GPCRs). These receptors are essential for various cellular signaling pathways that control processes like cell growth, differentiation, and response to extracellular signals. Hrs acts as an adaptor protein that helps mediate the sorting of activated receptors into intracellular compartments, allowing them to be either recycled to the cell surface or targeted for degradation in lysosomes.
Hrs inhibitors, therefore, disrupt these crucial intracellular sorting processes by binding to Hrs and preventing its normal function. This interference can have a profound impact on cell signaling and receptor regulation. By inhibiting Hrs, these compounds alter the dynamics of cell surface receptor levels, leading to downstream effects on cellular responses to growth factors, hormones, and other signaling molecules. Understanding the mechanisms and consequences of Hrs inhibition can provide valuable insights into the fundamental processes of receptor trafficking and cellular communication.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
This compound inhibits mTOR, a kinase involved in various cellular processes including autophagy, potentially impacting Hrs function. | ||||||
Bafilomycin A1 | 88899-55-2 | sc-201550 sc-201550A sc-201550B sc-201550C | 100 µg 1 mg 5 mg 10 mg | $98.00 $255.00 $765.00 $1457.00 | 280 | |
This is a specific inhibitor of vacuolar-type H+-ATPase, affecting endosomal acidification, which could disrupt Hrs function. | ||||||
Autophagy Inhibitor, 3-MA | 5142-23-4 | sc-205596 sc-205596A | 50 mg 500 mg | $65.00 $261.00 | 113 | |
A known autophagy inhibitor that could indirectly affect Hrs function by disrupting autophagic processes. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
This is a PI3 kinase inhibitor that could potentially disrupt Hrs function by affecting endosomal signaling and trafficking. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $69.00 | 2 | |
Known to elevate lysosomal pH, chloroquine could disrupt endosomal sorting and potentially Hrs function. | ||||||
Dynamin Inhibitor I, Dynasore | 304448-55-3 | sc-202592 | 10 mg | $89.00 | 44 | |
A non-competitive inhibitor of dynamin, dynasore could affect endocytosis and subsequently Hrs function. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor, LY294002 could disrupt various signaling pathways, potentially impacting Hrs activity. | ||||||
U 18666A | 3039-71-2 | sc-203306 sc-203306A | 10 mg 50 mg | $143.00 $510.00 | 2 | |
This compound disrupts cholesterol trafficking, which could influence membrane dynamics and Hrs localization or function. | ||||||
SB 202190 | 152121-30-7 | sc-202334 sc-202334A sc-202334B | 1 mg 5 mg 25 mg | $31.00 $128.00 $454.00 | 45 | |
A p38 MAP kinase inhibitor, SB202190 could affect various signaling pathways, potentially altering Hrs expression or stability. | ||||||
Spautin-1 | 1262888-28-7 | sc-507306 | 10 mg | $168.00 | ||
Known to promote the degradation of PI3K, Spautin-1 could indirectly impact Hrs function by affecting endosomal trafficking. | ||||||