Erasin inhibitors are a class of chemical compounds that specifically target and inhibit the function of the erasin protein, which is associated with the endoplasmic reticulum (ER)-associated degradation (ERAD) pathway. ERAD is a crucial cellular process responsible for identifying, ubiquitinating, and degrading misfolded or unassembled proteins within the ER to maintain cellular homeostasis. Erasin is believed to play an essential role in facilitating the clearance of these misfolded proteins by acting as a molecular scaffold or interacting with other ERAD components, such as ubiquitin ligases and chaperones. By inhibiting erasin, researchers can study its specific contribution to the ERAD pathway and how its function influences protein quality control within the ER.
The mechanism of erasin inhibitors likely involves binding to critical domains of the erasin protein, blocking its ability to interact with key partners involved in ERAD, such as ubiquitin-conjugating enzymes or protein substrates marked for degradation. Structurally, erasin inhibitors may mimic natural substrates or binding motifs, enabling them to competitively block the regions essential for erasin's function in the degradation process. These inhibitors can provide valuable insights into the molecular mechanisms that regulate ERAD and the maintenance of protein homeostasis in the ER. By studying erasin inhibitors, researchers can better understand how disruptions in protein degradation contribute to cellular stress responses, protein misfolding, and the overall dynamics of ER function. This knowledge is fundamental for gaining a deeper understanding of how cells manage protein quality control and maintain proper folding environments under various physiological conditions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
A potent kinase inhibitor that can modulate various signaling pathways potentially linked with the activity of "erasin". | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $82.00 $216.00 $416.00 | 48 | |
Selectively inhibits the TGF-β type I receptor ALK5, which could alter "erasin" activity if involved in TGF-β signaling. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
Inhibits PI3K, potentially affecting the PI3K/AKT pathway that "erasin" may participate in. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $153.00 $356.00 | 15 | |
Aurora kinase inhibitor, could disrupt cell cycle regulation potentially involving "erasin". | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Inhibits mTOR and can affect the translation of proteins in pathways associated with "erasin". | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
Induces ER stress which can impact calcium homeostasis, potentially affecting "erasin"-mediated signaling. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Proteasome inhibitor that can stabilize proteins and potentially influence the degradation of "erasin" or its associated regulatory proteins. | ||||||
Cyclopamine | 4449-51-8 | sc-200929 sc-200929A | 1 mg 5 mg | $94.00 $208.00 | 19 | |
Inhibits the Hedgehog signaling pathway, which could influence "erasin" if it is part of this pathway. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
A DNA methyltransferase inhibitor that could affect the expression levels of "erasin" by altering gene expression. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
Histone deacetylase inhibitor that can alter chromatin structure and gene expression levels of proteins including "erasin". | ||||||