Membralin inhibitors are a class of chemical compounds that primarily target a specific protein known as membralin. These inhibitors have gained significant attention in the field of molecular biology and pharmacology due to their potential role in modulating cellular processes. Membralin itself is a transmembrane protein localized in the endoplasmic reticulum (ER) of eukaryotic cells. It plays a crucial role in regulating the ER-associated protein degradation (ERAD) pathway, which is responsible for disposing of misfolded or surplus proteins. The ERAD pathway is essential for maintaining cellular homeostasis and preventing the accumulation of toxic protein aggregates within the ER. Membralin inhibitors, as the name suggests, interfere with the normal function of membralin, thereby affecting the ERAD pathway and influencing various downstream cellular events.
These inhibitors typically function by binding to membralin and disrupting its interaction with other ERAD-associated proteins, such as Derlin-1 and HRD1. This disruption can lead to the impairment of the ERAD pathway, causing a buildup of misfolded proteins and an unfolded protein response (UPR) in the cell. The UPR is a cellular stress response mechanism that aims to restore ER homeostasis but can also trigger apoptosis if the stress is overwhelming or prolonged. Membralin inhibitors, by interfering with the ERAD pathway, can have diverse effects on cellular processes, including protein quality control, cellular stress response, and potentially even cell fate decisions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
GSK 2606414 | 1337531-36-8 | sc-490182 sc-490182A | 5 mg 25 mg | $163.00 $572.00 | ||
A potent and selective inhibitor of PERK, one of the main transducers of the UPR, hence affects TMEM259 indirectly by modulating UPR. | ||||||
Salubrinal | 405060-95-9 | sc-202332 sc-202332A | 1 mg 5 mg | $34.00 $104.00 | 87 | |
Targets eIF2α phosphatases, indirectly influencing the UPR and might affect TMEM259 function as a result. | ||||||
ISRIB | 1597403-47-8 | sc-488404 | 10 mg | $300.00 | 1 | |
A molecule that modulates the integrated stress response, potentially affecting the pathways TMEM259 is involved in. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $172.00 $305.00 | 66 | |
Induces ER stress by inhibiting N-linked glycosylation, thus altering the UPR and consequently could affect TMEM259 indirectly. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
A SERCA pump inhibitor that induces ER stress and the UPR, potentially impacting TMEM259's role indirectly. | ||||||
4-Phenylbutyric acid | 1821-12-1 | sc-232961 sc-232961A sc-232961B | 25 g 100 g 500 g | $53.00 $136.00 $418.00 | 10 | |
A chemical chaperone that reduces protein misfolding and UPR, thereby might indirectly impact TMEM259. | ||||||
Guanabenz HCl | 23113-43-1 | sc-507500 | 100 mg | $246.00 | ||
Alters eIF2α signaling, thus indirectly affecting the UPR and could influence TMEM259 function. | ||||||
Sephin1 | 13098-73-2 | sc-507502 | 5 mg | $578.00 | ||
Selective inhibitor of phosphatase complexes that modulate the UPR, could indirectly affect TMEM259. | ||||||
Nelfinavir | 159989-64-7 | sc-507314 | 10 mg | $168.00 | ||
Although primarily known for other actions, it has been shown to induce ER stress and modulate UPR, hence might affect TMEM259 indirectly. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
A proteasome inhibitor that induces ER stress and UPR, potentially impacting TMEM259's function indirectly. | ||||||