Date published: 2026-5-21

1-800-457-3801

SCBT Portrait Logo
Seach Input

FRP-3 Activators

Regarding the chemical class FRP-3 Activators, these are chemicals that can act as indirect activators of FRP-3 (Secreted frizzled-related protein 3) by influencing related pathways or cellular processes, notably the Wnt/β-catenin pathway, MAPK pathway, and PI3K/AKT pathway. These pathways are crucial in several biological processes including cell proliferation, differentiation, and survival. FRP-3, being an antagonist of Wnt proteins, has a significant role in the modulation of these pathways.

The chemicals in this class are either inhibitors or activators of various components of these pathways. For instance, Lithium Chloride, CHIR-99021, JW-55, and Y-27632 are known to activate the Wnt/β-catenin pathway, thereby indirectly influencing FRP-3. On the other hand, SB-431542, PD-0325901, LY-294002, Rapamycin, SP-600125, XAV-939, Roscovitine, and Salinomycin are inhibitors of different components of these pathways, which can indirectly influence FRP-3 by perturbing the balance between pathways or upregulating the Wnt/β-c-catenin signaling. These chemicals act on various targets, including GSK-3 beta, TGF-beta receptors, MEK, ROCK, PI3K, mTOR, JNK, tankyrase, CDKs, and Wnt/β-catenin signaling. Influence on these pathways by these chemicals leads to changes in the activity of FRP-3. For example, chemicals that inhibit components of the Wnt/β-catenin pathway can increase the antagonistic action of FRP-3 on Wnt proteins. Conversely, chemicals that activate the Wnt/β-catenin pathway may lead to a decrease in the antagonistic function of FRP-3. It's important to note that the indirect activation of FRP-3 by these chemicals is a result of their primary action on various other pathway components. The specific effect on FRP-3 will depend upon the balance of these pathways in specific cellular contexts and the degree of modulation by these chemicals.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lithium

7439-93-2sc-252954
50 g
$214.00
(0)

Lithium Chloride inhibits GSK3β, a key enzyme in the Wnt/β-catenin pathway that promotes β-catenin degradation. By inhibiting GSK3β, Lithium Chloride can stabilize β-catenin, enhancing the Wnt/β-catenin pathway and indirectly reducing the inhibitory effect of FRP-3.

GSK-3 Inhibitor IX

667463-62-9sc-202634
sc-202634A
sc-202634B
1 mg
10 mg
50 mg
$58.00
$188.00
$884.00
10
(1)

BIO is a potent and selective inhibitor of GSK3β, similar to Lithium Chloride. It stabilizes β-catenin, promoting the Wnt/β-catenin pathway and indirectly mitigating the inhibitory role of FRP-3.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$110.00
$250.00
$936.00
$50.00
33
(2)

Quercetin is a flavonoid compound that inhibits the Wnt/β-catenin pathway by promoting β-catenin degradation, similar to Niclosamide. This can indirectly enhance the inhibitory role of FRP-3.

JW 55

664993-53-7sc-364517
sc-364517A
10 mg
50 mg
$172.00
$726.00
(0)

JW 55 is a small molecule that promotes the interaction between β-catenin and the destruction complex, leading to its degradation and the inhibition of the Wnt/β-catenin pathway. This can indirectly enhance the inhibitory role of FRP-3.

Pyrvinium Pamoate

3546-41-6sc-476920A
sc-476920
250 mg
500 mg
$228.00
$422.00
(0)

Pyrvinium Pamoate is an anthelmintic drug that has been found to inhibit the Wnt/β-catenin pathway by enhancing the activity of casein kinase 1α (CK1α), which promotes β-catenin degradation. This can indirectly enhance the inhibitory role of FRP-3.

Cardamonin

19309-14-9sc-293984
sc-293984A
10 mg
50 mg
$224.00
$940.00
(1)

Cardamonin is a flavonoid compound that inhibits the Wnt/β-catenin pathway by promoting β-catenin degradation, similar to Quercetin and Niclosamide. This can indirectly enhance the inhibitory role of FRP-3.

PRI-724

1422253-38-0sc-507535
25 mg
$260.00
(0)

PRI-724 inhibits the interaction between β-catenin and CBP, like ICG-001, inhibiting the Wnt/β-catenin pathway and indirectly enhancing the inhibitory role ofFRP-3.