Date published: 2025-12-15

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BRAF35 Inhibitors

BRAF35, also known as B-raf proto-oncogene, is a protein encoded by the BRAF gene and is a crucial component of the MAPK signaling pathway. This pathway plays a central role in regulating cellular processes such as cell proliferation, differentiation, and survival. BRAF35 functions as a serine/threonine kinase, and its activity is tightly regulated to ensure proper cellular responses to extracellular signals. Upon activation, BRAF35 phosphorylates downstream targets, including MEK1 and MEK2, leading to the activation of the ERK1/2 kinases, which subsequently modulate gene expression and cellular functions. Inhibition of BRAF35 involves targeting its kinase activity to prevent aberrant signaling through the MAPK pathway, particularly in the context of cancer. Mechanistically, inhibition can be achieved through small molecule inhibitors that directly bind to the ATP-binding pocket of BRAF35, thereby preventing its kinase activity and downstream signaling. Additionally, inhibition may also involve targeting upstream regulators of BRAF35 activation or signaling, such as growth factor receptors or RAS proteins, to indirectly suppress BRAF35 activity. Furthermore, modulation of scaffolding proteins or signaling complexes involved in the assembly and activation of the MAPK pathway may also represent alternative strategies for inhibiting BRAF35 and attenuating MAPK signaling.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Dabrafenib

1195765-45-7sc-364477
sc-364477A
sc-364477B
sc-364477C
sc-364477D
5 mg
25 mg
50 mg
100 mg
10 g
$138.00
$255.00
$273.00
$403.00
$12240.00
6
(1)

Another selective inhibitor of mutant BRAF(V600E), also targeting the ATP-binding site, disrupting MAPK pathway activation.

Encorafenib

1269440-17-6sc-507422
1 mg
$115.00
(0)

Yet another ATP-competitive inhibitor of BRAF(V600E) mutant, blocking MAPK signaling to inhibit cell proliferation.

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

Multikinase inhibitor with activity against BRAF, VEGFR, and PDGFR, disrupting tumor angiogenesis and growth signaling pathways.

Regorafenib

755037-03-7sc-477163
sc-477163A
25 mg
50 mg
$320.00
$430.00
3
(0)

Broad-spectrum kinase inhibitor, targeting BRAF and other kinases involved in angiogenesis and tumor progression.

Vemurafenib

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

A specific inhibitor of mutant BRAF(V600E) with research application in melanoma therapy by suppressing MAPK pathway activation.

Raf Kinase Inhibitor V

918505-84-7sc-222241
sc-222241A
1 mg
10 mg
$198.00
$480.00
2
(2)

Another BRAF(V600E) inhibitor, structurally related to Vemurafenib, impeding MAPK signaling and tumor cell growth.

RAF265

927880-90-8sc-364599
5 mg
$191.00
(0)

A multi-kinase inhibitor, targeting RAF kinases including BRAF, to inhibit MAPK signaling and tumor cell proliferation.

LY3009120

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

Potent and selective BRAF inhibitor, blocking aberrant MAPK pathway activation by BRAF mutations, and used in research.

TAK 632

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

Small molecule inhibitor of BRAF kinase, hampering MAPK signaling activation in cancer cells harboring BRAF mutations.