Date published: 2026-4-1

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PCDHAC Activators

The chemical class known as PCDHAC activators encompasses a diverse range of compounds that can influence the expression or function of protocadherin alpha (PCDHAC) proteins. These activators do not bind directly to the PCDHAC proteins but instead exert their influence through modulation of various cellular signaling pathways and epigenetic mechanisms that can lead to changes in PCDHAC activity. One avenue through which these activators operate is by altering intracellular levels of second messengers such as cyclic AMP (cAMP). Compounds that increase intracellular cAMP can activate protein kinase A (PKA), which then phosphorylates transcription factors and other proteins involved in the regulation of gene expression, including genes coding for PCDHAC. These changes in gene expression can result in increased synthesis of PCDHAC proteins and thus modulate cellular adhesion processes.

Another method by which PCDHAC activators can exert their effect is through epigenetic modifications. Certain compounds can inhibit enzymes like histone deacetylases and DNA methyltransferases, leading to a more open chromatin structure and decreased methylation of DNA, respectively. These epigenetic alterations can enhance the transcription of genes, including those related to PCDHAC proteins. Furthermore, changes in intracellular calcium levels can also affect PCDHAC activity, as calcium ionophores increase the availability of calcium ions, which are crucial for the function of calcium-dependent adhesion molecules like PCDHACs. Collectively, these compounds can regulate the intricate network of cellular signals that govern the expression and function of PCDHAC proteins, which play a vital role in cell-to-cell communication and adhesion.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

Calcium ionophores elevate intracellular calcium concentration, which could activate the calcium-dependent adhesion properties of PCDHA proteins.

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$41.00
$132.00
$214.00
$500.00
$948.00
119
(6)

PMA activates protein kinase C (PKC), which can modulate signaling pathways that could activate the expression of PCDHA proteins.

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)

Retinoic acid regulates gene expression and could activate PCDHA proteins by influencing neuronal differentiation pathways.

Lithium

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

Lithium chloride inhibits glycogen synthase kinase-3 (GSK-3), which could stabilize proteins that regulate PCDHA gene expression.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

TSA is a histone deacetylase inhibitor that can promote chromatin remodeling, potentially increasing PCDHA gene expression.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

This DNA methyltransferase inhibitor may lead to demethylation of PCDHA gene promoters, enhancing PCDHA expression.

Dibutyryl-cAMP

16980-89-5sc-201567
sc-201567A
sc-201567B
sc-201567C
20 mg
100 mg
500 mg
10 g
$47.00
$136.00
$492.00
$4552.00
74
(7)

db-cAMP is a cell-permeable cAMP analog that can mimic the effect of cAMP, potentially influencing PCDHA protein expression.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$31.00
$47.00
$84.00
$222.00
19
(3)

Sodium butyrate is a histone deacetylase inhibitor that can affect gene expression, which may include upregulation of PCDHA proteins.

Calcium dibutyryladenosine cyclophosphate

362-74-3sc-482205
25 mg
$147.00
(0)

dbcAMP is a cAMP analog that may upregulate PCDHA expression through pathways influenced by cAMP levels.

Valproic Acid

99-66-1sc-213144
10 g
$87.00
9
(1)

Valproic acid is a histone deacetylase inhibitor that might increase PCDHA protein expression by altering chromatin structure.