Date published: 2025-12-18

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Raf-B Inhibitors

Raf-B inhibitors belong to a significant category of chemical compounds that play a pivotal role in modulating cellular signaling pathways. These inhibitors are specifically designed to target the activity of Raf-B, a kinase enzyme that is a part of the larger Raf family of kinases. Kinases are enzymes responsible for phosphorylating target proteins, thereby regulating various cellular processes. Raf-B, in particular, is implicated in pathways related to cell growth, proliferation, and differentiation. The development of Raf-B inhibitors stems from the recognition of its involvement in the mitogen-activated protein kinase (MAPK) signaling pathway, which plays a fundamental role in transmitting extracellular signals to the nucleus, ultimately influencing gene expression. Structurally, Raf-B inhibitors exhibit distinct molecular arrangements that enable them to interact with the active site of the Raf-B enzyme. These compounds often possess a combination of hydrophobic and hydrogen-bonding moieties that facilitate their binding to specific residues within the enzyme's active pocket. This interaction effectively disrupts the enzymatic activity of Raf-B, leading to downstream effects on the MAPK pathway. Researchers have harnessed the insights gained from studying Raf-B inhibitors to gain a deeper understanding of intracellular communication networks and their impact on cellular behavior. By manipulating the activity of Raf-B through these inhibitors, scientists have unlocked valuable information about the intricate interplay between various signaling cascades. In summary, Raf-B inhibitors constitute a significant class of compounds with the capacity to modulate the activity of the Raf-B kinase enzyme. Through their targeted interaction with the enzyme's active site, these inhibitors provide a valuable tool for investigating cellular signaling pathways and the broader mechanisms that govern cellular responses to extracellular cues.

Items 11 to 17 of 17 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Vemurafenib

918504-65-1sc-364643
sc-364643A
10 mg
50 mg
$115.00
$415.00
11
(1)

Binds to BRAF V600E mutant, inhibiting the MAPK signaling pathway in cancer cells.

Cobimetinib

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

Selectively inhibits MEK1/2, downstream of RAF, in the MAPK pathway.

Trametinib

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

Targets MEK1/2, hindering cell growth and proliferation in cancers.

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)

Blocks MEK1/2, leading to inhibition of tumor growth and angiogenesis.

BAY 869766

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

Inhibits MEK1/2, preventing activation of downstream signaling cascades in cancer.

TAK 632

1228591-30-7sc-473801
5 mg
$224.00
(0)

Targets MEK and BRAF, impeding MAPK signaling and cell proliferation.

LY3009120

1454682-72-4sc-507538
5 mg
$125.00
(0)

Inhibits both RAF and MEK kinases, disrupting the MAPK pathway in cancer cells.