Date published: 2026-4-24

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GIT2 Inhibitors

GIT2 inhibitors belong to a specific chemical class of compounds that are designed to selectively and potently inhibit the activity of G protein-coupled receptor kinase interacting protein 2 (GIT2). GIT2 is a key regulator of intracellular signaling pathways and plays a critical role in various cellular processes. The inhibitors of this class are designed to specifically bind to the active site of GIT2, its normal function and interfering with its ability to modulate downstream signaling cascades. By inhibiting GIT2, these compounds aim to disrupt the intricate balance of cellular signaling, potentially leading to altered cellular responses and physiological outcomes. GIT2 inhibitors are chemically synthesized substances that have been extensively studied for their mechanism of action and have shown promising effects in research. Further research is required to fully understand the precise cellular and molecular consequences of GIT2 inhibition and explore their potential applications in various fields.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$57.00
$100.00
$250.00
129
(3)

Sorafenib is a multi-kinase inhibitor that targets various receptors, including VEGFR, PDGFR, and RAF kinases. Inhibition of these kinases can alter GIT2-related signaling pathways, particularly those involved in cell proliferation and survival.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$70.00
$145.00
51
(1)

Dasatinib is a tyrosine kinase inhibitor that primarily targets BCR-ABL and Src family kinases. It can affect GIT2-related pathways by modulating downstream signaling of integrins and other membrane receptors that engage GIT2.

Nilotinib

641571-10-0sc-202245
sc-202245A
10 mg
25 mg
$209.00
$413.00
9
(1)

Nilotinib is a selective inhibitor of BCR-ABL kinase, which can indirectly affect GIT2 signaling by altering the balance of downstream pathways that may intersect with GIT2 regulatory networks.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

LY294002 is a PI3K inhibitor that impacts the AKT/PKB signaling pathway. Since GIT2 can interact with components of the PI3K pathway, inhibition of PI3K can modulate GIT2-associated cellular functions.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

PD98059 is a MEK inhibitor that prevents the activation of MAPK/ERK. It can influence GIT2 activity by altering the MAPK signaling cascade, which is potentially linked to GIT2 functions.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

SP600125 is an inhibitor of JNK, which may impact GIT2 signaling by modulating stress- and inflammation-related pathways where GIT2 might play a role.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Wortmannin is a potent and irreversible inhibitor of PI3K, which can affect GIT2 signaling through its role in membrane trafficking and signal transduction pathways associated with GIT2.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Rapamycin is an mTOR inhibitor that can indirectly influence GIT2 by modulating the mTOR signaling pathways involved in cell growth, proliferation, and survival.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

Y-27632 is a ROCK inhibitor that can affect GIT2 signaling by altering the actin cytoskeleton dynamics and cell motility processes where GIT2 is implicated.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$94.00
$227.00
30
(1)

PP2 is an Src family kinase inhibitor that can modulate GIT2 signaling pathways by affecting integrin signaling and cytoskeletal organization.