Date published: 2026-4-23

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FLRT2 Activators

The chemical class known as FLRT2 Activators comprises a diverse array of compounds that indirectly influence the activity of FLRT2 (Fibronectin Leucine Rich Transmembrane Protein 2), a protein involved in cell adhesion, tissue development, and cell communication pathways. This class is characterized not by direct interaction with FLRT2, but rather by the modulation of various signaling pathways that intersect with the functional role of FLRT2 in cellular processes. Key components in this class include growth factors such as Epidermal Growth Factor (EGF) and Fibroblast Growth Factor (FGF), both of which are crucial in cell proliferation and tissue development processes. EGF, through its action on the EGFR signaling pathway, and FGF, with its role in developmental processes, are hypothesized to indirectly impact the cellular environments where FLRT2 functions. Additionally, this class encompasses agonists of several critical signaling pathways like Wnt, Hedgehog, TGF-beta, BMP (Bone Morphogenetic Proteins), Notch, and PDGF (Platelet-Derived Growth Factor). These signaling molecules and pathways play pivotal roles in tissue patterning, cell fate determination, and developmental processes, suggesting a potential overlap with FLRT2's involvement in these areas.

Furthermore, the FLRT2 Activators class includes compounds like Retinoic Acid, Lithium Chloride, Nitric Oxide Donors, and Calcium Ionophores. Retinoic Acid, involved in cell differentiation, could influence FLRT2's role in developmental pathways. Lithium Chloride, known to impact Wnt signaling, offers another potential route through which FLRT2 activity could be modulated. Nitric Oxide Donors and Calcium Ionophores, by altering intracellular signaling dynamics, can also contribute to the regulation of pathways relevant to FLRT2's function. The inclusion of these diverse chemicals underscores the complex nature of cellular signaling networks and the myriad ways in which these networks can be influenced. Collectively, this chemical class represents a multifaceted approach to modulating the cellular and molecular context in which FLRT2 operates, highlighting the intricate interplay of signaling pathways in regulating key cellular functions such as adhesion, communication, and tissue development. The indirect impact of these activators on FLRT2 exemplifies the complexity of targeting specific proteins within the broad tapestry of cellular signaling.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

NOC-18

146724-94-9sc-202247
sc-202247A
sc-202247B
sc-202247C
10 mg
50 mg
100 mg
500 mg
$51.00
$184.00
$305.00
$1122.00
18
(1)

NOC-18 releases nitric oxide (NO) in a controlled manner, which can indirectly activate FLRT2 by S-nitrosylation of cysteine residues on or near the protein. This post-translational modification may lead to changes in FLRT2 conformation, enhancing its interaction with binding partners and promoting its activation-related signaling pathways.

A23187

52665-69-7sc-3591
sc-3591B
sc-3591A
sc-3591C
1 mg
5 mg
10 mg
25 mg
$55.00
$131.00
$203.00
$317.00
23
(1)

A23187 acts as a mobile ion carrier that facilitates the influx of calcium ions (Ca2+) into the cell. Elevated intracellular Ca2+ levels can indirectly activate FLRT2 by triggering signaling cascades that lead to the phosphorylation of proteins involved in FLRT2's activation or by altering the local cellular environment in a way that promotes FLRT2's active conformation or its interaction with other signaling molecules.

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$66.00
$325.00
$587.00
$1018.00
28
(1)

All-trans Retinoic Acid (atRA) binds to nuclear retinoic acid receptors (RARs), which then regulate gene expression by acting as transcription factors. This regulation can lead to the upregulation of genes involved in the activation of FLRT2, either by increasing the expression of FLRT2 itself or by enhancing the expression of proteins that interact with and activate FLRT2.

Lithium

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

Lithium Chloride inhibits glycogen synthase kinase 3 (GSK-3), a kinase involved in the phosphorylation and inactivation of various proteins. Inhibition of GSK-3 by Lithium Chloride can lead to the stabilization and activation of β-catenin, which may indirectly enhance FLRT2 activation by promoting gene expression patterns favorable to FLRT2's activation or by stabilizing cellular structures that facilitate FLRT2 signaling.