Date published: 2025-10-25

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MEK-4 Inhibitors

The mitogen-activated protein kinase (MAPK) pathways are pivotal signaling cascades involved in a variety of cellular processes such as proliferation, differentiation, and apoptosis. Central to the MAPK pathways are the MEK (Mitogen-activated protein kinase kinase) proteins, which are dual-specificity protein kinases that phosphorylate and activate their respective MAP kinases. The MEK family consists of several members, among which MEK-4 stands out due to its unique role and regulation mechanism. MEK-4 inhibitors, as their name suggests, are molecules designed to target and inhibit the activity of the MEK-4 enzyme. By doing so, they can modulate the downstream signaling events controlled by this kinase. The chemical structures of MEK-4 inhibitors can vary widely, encompassing small molecules, peptides, and even biologics. Their mechanism of action usually involves binding to the catalytic or allosteric sites of the MEK-4 enzyme, thus preventing it from phosphorylating its substrate MAP kinases. The specificity and selectivity of these inhibitors are crucial to ensure that only MEK-4 is targeted, without affecting the broader kinome, which can lead to off-target effects and undesired cellular outcomes. Advances in structural biology and computational chemistry have played a significant role in the design and optimization of MEK-4 inhibitors, allowing researchers to fine-tune their interactions with the kinase and improve their efficiency. As such, these inhibitors are valuable tools in the study of cellular signaling and the intricate web of regulatory mechanisms that maintain cellular homeostasis.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

3′,4′,7-Trihydroxyisoflavone

485-63-2sc-206722
200 mg
$295.00
1
(1)

3',4',7-Trihydroxyisoflavone (CAS 485-63-2) is a chemical compound belonging to the isoflavone class, characterized by its three hydroxy groups attached to its structure. Studies have identified it as an inhibitor of MEK-4, a kinase involved in various cellular signaling pathways. This inhibition can impact cell proliferation, differentiation, and other processes influenced by the MEK-4 pathway.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$63.00
$241.00
136
(2)

U0126 is a well-known inhibitor of MEK1/2, preventing their activation by upstream kinases, which leads to reduced ERK phosphorylation and downstream signaling.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$39.00
$90.00
212
(2)

PD98059 is another MEK1/2 inhibitor, which works by binding to the inactive forms of MEK1/2, preventing their activation and subsequent ERK phosphorylation.

Selumetinib

606143-52-6sc-364613
sc-364613A
sc-364613B
sc-364613C
sc-364613D
5 mg
10 mg
100 mg
500 mg
1 g
$28.00
$80.00
$412.00
$1860.00
$2962.00
5
(1)

Selumetinib is a potent, selective, non-ATP competitive inhibitor of MEK1/2, and it has been studied in various trials.

Trametinib

871700-17-3sc-364639
sc-364639A
sc-364639B
5 mg
10 mg
1 g
$112.00
$163.00
$928.00
19
(1)

Trametinib is a compound inhibiting MEK1/2 and thus interrupting the MAPK/ERK signaling pathway.

Cobimetinib

934660-93-2sc-507421
5 mg
$270.00
(0)

Cobimetinib is another MEK inhibitor used in combination with other compounds by inhibiting MEK1/2 activity.

MEK 162

606143-89-9sc-488879
10 mg
$306.00
(0)

Binimetinib is a selective inhibitor of MEK1/2 and it works by inhibiting the MAPK/ERK pathway.

TAK-733

1035555-63-5sc-364630
sc-364630A
5 mg
10 mg
$340.00
$640.00
1
(0)

TAK-733 is an experimental MEK inhibitor that has shown potential in research studies for its ability to inhibit MEK1/2 and affect tumor growth.

BAY 869766

923032-37-5sc-364427
sc-364427A
5 mg
10 mg
$240.00
$420.00
1
(1)

BAY 869766 is a potent and selective MEK1/2 inhibitor that has undergone clinical evaluation for its potential therapeutic purposes