Date published: 2025-12-8

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DCC Inhibitors

The chemical class of DCC inhibitors encompasses a diverse range of compounds that intricately modulate the activity of DCC (Deleted in Colorectal Cancer). Among these, RO-31-8220 stands out as a protein kinase inhibitor with activity against multiple kinases, influencing DCC by modulating downstream signaling cascades involved in cellular processes, particularly axon guidance. The compound impacts intracellular pathways related to DCC, altering the cellular responses to guidance cues during axon navigation. Several other inhibitors, such as Y27632 (ROCK inhibitor), PP2 (Src family kinase inhibitor), PD98059 (MEK inhibitor), and SU5402 (FGFR inhibitor), indirectly influence DCC-mediated axon guidance pathways. Y27632 alters Rho/ROCK signaling, impacting DCC in cellular motility, while PP2 modulates Src-dependent signaling implicated in axon guidance processes. PD98059 and SU5402, respectively, dampen the MAPK and FGFR-dependent pathways, affecting DCC in the context of axon guidance.

Wortmannin and LY294002, both PI3K inhibitors, impact DCC indirectly by suppressing PI3K-dependent pathways involved in axon guidance. SB-431542, a TGF-β receptor inhibitor, affects TGF-β-dependent signaling pathways, indirectly influencing DCC in processes related to axon guidance. JNK Inhibitor II targets c-Jun N-terminal kinases, modulating DCC through JNK-dependent signaling pathways related to axon guidance. CHIR-99021, a GSK-3 inhibitor, and U0126, another MEK inhibitor, impact DCC-mediated axon guidance pathways by modulating the activity of GSK-3 and dampening the MAPK pathway, respectively. Lastly, GW5074, a c-Raf inhibitor, influences DCC indirectly by inhibiting c-Raf-dependent signaling pathways involved in axon guidance. In conclusion, this comprehensive class of DCC inhibitors provides valuable insights into the intricate regulatory networks involved in modulating DCC's role in axon guidance. Each compound, through specific pathways and mechanisms, can intricately influence the dynamics of DCC, shedding light on avenues for conditions where DCC dysregulation plays a role.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Ro 31-8220

138489-18-6sc-200619
sc-200619A
1 mg
5 mg
$90.00
$240.00
17
(1)

A protein kinase inhibitor targeting multiple kinases, indirectly influencing DCC by modulating downstream signaling cascades.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$92.00
$223.00
30
(1)

Src family kinase inhibitor, indirectly affecting DCC by modulating Src-dependent signaling pathways implicated in axon guidance.

PD 98059

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

MEK inhibitor dampening the MAPK pathway, influencing DCC through downstream modulation of MAPK signaling in axon guidance processes.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$66.00
$219.00
$417.00
97
(3)

PI3K (Phosphoinositide 3-kinase) inhibitor impacting DCC indirectly by suppressing PI3K-dependent pathways involved in axon guidance.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

Another PI3K inhibitor, impacting DCC-mediated pathways in axon guidance by modulating the PI3K signaling cascade.

Casein Kinase I Inhibitor, D4476

301836-43-1sc-202522
1 mg
$97.00
6
(1)

TGF-β receptor inhibitor affecting TGF-β-dependent signaling, indirectly influencing DCC in processes related to axon guidance.

SP600125

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

Inhibitor of c-Jun N-terminal kinases (JNK), influencing DCC through modulation of JNK-dependent signaling pathways related to axon guidance.

GSK-3 Inhibitor XVI

252917-06-9sc-221691
sc-221691A
5 mg
25 mg
$153.00
$520.00
4
(1)

GSK-3 inhibitor impacting DCC-mediated axon guidance pathways by modulating the activity of GSK-3 and downstream signaling cascades.

GW 5074

220904-83-6sc-200639
sc-200639A
5 mg
25 mg
$106.00
$417.00
10
(1)

c-Raf inhibitor, indirectly affecting DCC through the inhibition of c-Raf-dependent signaling pathways involved in axon guidance.