Date published: 2025-9-17

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26S Proteasome Inhibitors

26S Proteasome Inhibitors comprises a group of compounds that exhibit the ability to hinder the enzymatic activity of the 26S proteasome complex, a crucial cellular machinery responsible for the selective degradation of proteins. The 26S proteasome is an intricate assembly composed of a 20S core particle and 19S regulatory particles on either end. The 20S core particle is further subdivided into α and β rings, each containing seven distinct subunits. The regulatory 19S particles assist in recognizing ubiquitinated target proteins and unfolding them for entry into the proteolytic chamber of the core particle. 26S proteasome inhibitors act by binding to specific active sites within the 20S core particle, thereby obstructing its proteolytic function. The ubiquitin-proteasome system plays a pivotal role in regulating cellular processes by controlling protein levels and quality. The inhibition of this system through 26S proteasome inhibitors results in the accumulation of targeted proteins within cells, leading to disruptions in various signaling pathways and biological processes. The inhibition process is intricate and highly selective, involving interactions between the inhibitor molecules and key residues within the proteasomal active sites.These inhibitors belong to a diverse chemical class, with varying structures and mechanisms of action. They can be small organic molecules or synthetic compounds engineered to interact with the proteasome's catalytic sites in distinct ways. The design and development of 26S proteasome inhibitors often rely on detailed knowledge of the proteasome's structural and functional characteristics, allowing researchers to tailor compounds for specific modes of inhibition. The exploration of this class of compounds has not only enhanced our understanding of cellular protein degradation but has also paved the way for applications in research, ranging from investigating protein turnover dynamics to understanding the regulation of complex cellular pathways. The study of 26S proteasome inhibitors is an ongoing area of research, with scientists continuously seeking to unravel their specific mechanisms of action and broaden our insights into cellular biology.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Bortezomib (CAS 179324-69-7) is a proteasome inhibitor that disrupts 26S proteasome function by binding to its catalytic sites, preventing targeted protein degradation.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$56.00
$260.00
$980.00
163
(3)

MG-132 (CAS 133407-82-6) is a proteasome inhibitor. It works as a reversible inhibitor of the 26S proteasome by binding to its active sites, hindering targeted protein breakdown.

MG-115

133407-86-0sc-221940
sc-221940A
1 mg
5 mg
$87.00
$220.00
3
(1)

MG-115 (CAS 133407-86-0) is a proteasome inhibitor. It functions by binding to the catalytic sites of the 26S proteasome, impeding the degradation of specific target proteins.

Carfilzomib

868540-17-4sc-396755
5 mg
$40.00
(0)

Carfilzomib selectively inhibits the chymotrypsin-like activity of the proteasome by irreversibly binding to its catalytic site. This disruption of protein degradation pathways promotes cell death in cancer cells.

Proteasome Inhibitor I

158442-41-2sc-3127
1 mg
$86.00
1
(0)

Proteasome Inhibitor I (CAS 158442-41-2) obstructs 26S proteasome function by targeting catalytic sites, impeding the degradation of specific proteins.

Ixazomib

1072833-77-2sc-489103
sc-489103A
10 mg
50 mg
$311.00
$719.00
(0)

Ixazomib acts as a reversible inhibitor of the 26S proteasome, targeting its β5 subunit and blocking protein degradation. This inhibition triggers apoptotic pathways in cancer cells.

Oprozomib

935888-69-0sc-477447
2.5 mg
$280.00
(0)

Oprozomib inhibits the 26S proteasome by binding to its active sites, preventing the degradation of ubiquitinated proteins. This leads to the accumulation of misfolded proteins and induces apoptosis in cancer cells.