Date published: 2025-10-15

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SCOCO Activators

SCOCO activators are a group of chemical compounds that have the potential to enhance its functional activity through their influence on specific signaling pathways. These compounds largely target the PI3K/AKT/mTOR and MAPK pathways, which are interconnected with the activity of SCOCO. PI3K inhibitors like LY294002, AKT inhibitor Triciribine, and mTOR inhibitors like Rapamycin, Apigenin, and WYE-354, can potentially enhance SCOCO activity through a compensatory mechanism when the PI3K/AKT/mTORpathway is inhibited.

Similarly, the MEK inhibitors PD98059, U0126, and Selumetinib, the JNK inhibitor SP600125, and the p38 MAPK inhibitor SB203580 can potentially affect SCOCO activity through a similar compensatory mechanism within the MAPK pathway. The rationale is that the inhibition of these pathways might result in an upregulation of SCOCO activity to maintain cellular equilibrium.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LY 294002

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

LY294002 is a potent inhibitor of phosphoinositide 3-kinases (PI3Ks), which are upstream regulators of AKT signaling pathway. SCOCO, known to interact with AKT, might get activated when the AKT pathway is affected. With LY294002 inhibiting PI3K, AKT activation will be dampened, potentially causing a compensatory increase in SCOCO activation to maintain cellular homeostasis.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

Rapamycin is an inhibitor of mammalian target of rapamycin (mTOR), a central regulator of cellular metabolism and growth. Since SCOCO is interconnected with the mTOR pathway through AKT, inhibition of mTOR by Rapamycin might cause a compensatory increase in SCOCO activation.

Triciribine

35943-35-2sc-200661
sc-200661A
1 mg
5 mg
$102.00
$138.00
14
(1)

Triciribine is an inhibitor of AKT, a key node in the PI3K/AKT/mTOR pathway. Since SCOCO is known to interact with AKT, inhibition of AKT might result in an upregulation of SCOCO activity to maintain cellular equilibrium.

PD 98059

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

PD98059 is an inhibitor of MEK, a kinase upstream of ERK in the MAPK pathway. As SCOCO interacts with AKT, which is also known to be influenced by cross-talk from the MAPK pathway, this could lead to enhanced SCOCO activity following MAPK pathway inhibition.

SP600125

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

SP600125 is a selective inhibitor of c-Jun N-terminal kinases (JNKs), which are members of the MAPK family. SCOCO, known to interact with AKT, might get indirectly activated when JNKs are inhibited due to the interconnectedness of signaling pathways.

SB 202190

152121-30-7sc-202334
sc-202334A
sc-202334B
1 mg
5 mg
25 mg
$30.00
$125.00
$445.00
45
(1)

SB203580 inhibits p38 MAPK, a member of the MAPK family. Inhibition of p38 could lead to enhanced SCOCO activity due to the interconnectedness of cellular signaling pathways and SCOCO's known interaction with AKT.

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 MEK1/2 inhibitor, which targets the MAPK pathway. The inhibition of this pathway could lead to enhanced SCOCO activity due to the cross-talk between the MAPK and AKT pathways, where SCOCO plays a role.

Apigenin

520-36-5sc-3529
sc-3529A
sc-3529B
sc-3529C
sc-3529D
sc-3529E
sc-3529F
5 mg
100 mg
1 g
5 g
25 g
100 g
1 kg
$32.00
$210.00
$720.00
$1128.00
$2302.00
$3066.00
$5106.00
22
(1)

Apigenin is a bioflavonoid that inhibits mTOR, a key component in the PI3K/AKT/mTOR pathway. By inhibiting mTOR, Apigenin might indirectly lead to enhanced SCOCO activity due to the interconnectedness of these signaling pathways.

WYE-354

1062169-56-5sc-364652
sc-364652A
10 mg
50 mg
$286.00
$1200.00
(0)

WYE-354 is an mTOR inhibitor that targets the PI3K/AKT/mTOR pathway. Inhibition of mTOR could lead to enhanced SCOCO activity due to the cross-talk between these signaling pathways.