Date published: 2026-5-30

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Membralin Inhibitors

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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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

GSK 2606414

1337531-36-8sc-490182
sc-490182A
5 mg
25 mg
$163.00
$572.00
(0)

A potent and selective inhibitor of PERK, one of the main transducers of the UPR, hence affects TMEM259 indirectly by modulating UPR.

Salubrinal

405060-95-9sc-202332
sc-202332A
1 mg
5 mg
$34.00
$104.00
87
(2)

Targets eIF2α phosphatases, indirectly influencing the UPR and might affect TMEM259 function as a result.

ISRIB

1597403-47-8sc-488404
10 mg
$300.00
1
(0)

A molecule that modulates the integrated stress response, potentially affecting the pathways TMEM259 is involved in.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$172.00
$305.00
66
(3)

Induces ER stress by inhibiting N-linked glycosylation, thus altering the UPR and consequently could affect TMEM259 indirectly.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$136.00
$446.00
114
(2)

A SERCA pump inhibitor that induces ER stress and the UPR, potentially impacting TMEM259's role indirectly.

4-Phenylbutyric acid

1821-12-1sc-232961
sc-232961A
sc-232961B
25 g
100 g
500 g
$53.00
$136.00
$418.00
10
(1)

A chemical chaperone that reduces protein misfolding and UPR, thereby might indirectly impact TMEM259.

Guanabenz HCl

23113-43-1sc-507500
100 mg
$246.00
(0)

Alters eIF2α signaling, thus indirectly affecting the UPR and could influence TMEM259 function.

Sephin1

13098-73-2sc-507502
5 mg
$578.00
(0)

Selective inhibitor of phosphatase complexes that modulate the UPR, could indirectly affect TMEM259.

Nelfinavir

159989-64-7sc-507314
10 mg
$168.00
(0)

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]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

A proteasome inhibitor that induces ER stress and UPR, potentially impacting TMEM259's function indirectly.