Date published: 2026-4-1

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ZNF358 Activators

ZNF358 play a pivotal role in its functional activation through various molecular mechanisms, primarily via the modulation of the cAMP-PKA signaling pathway. Forskolin, a potent adenylyl cyclase stimulator, directly increases intracellular cAMP levels, leading to the activation of protein kinase A (PKA). PKA then phosphorylates ZNF358, which is a crucial step in its functional activation. Similarly, Isoproterenol, a synthetic catecholamine, and Epinephrine, a natural catecholamine, both bind to beta-adrenergic receptors, triggering a cascade that also culminates in cAMP elevation and PKA activation. Prostaglandin E2 (PGE2), through its interaction with G-protein coupled receptors, and Cholera toxin, by irreversibly activating the Gs alpha subunit, both lead to sustained increases in cAMP levels, further promoting PKA-mediated phosphorylation of ZNF358.

8-Bromo-cAMP and Dibutyryl-cAMP, both of which are cAMP analogs that resist degradation and thereby sustain PKA activation. IBMX and Rolipram, by inhibiting phosphodiesterases that break down cAMP, lead to an accumulation of cAMP within the cell, amplifying PKA activity and subsequent phosphorylation of ZNF358. Zaprinast, though primarily known as a PDE5 inhibitor, can also contribute to elevated cAMP and/or cGMP levels, potentially enhancing PKA activation. Beyond the cAMP-PKA axis, PMA, an activator of protein kinase C (PKC), may initiate alternative phosphorylation pathways, while Anisomycin, by activating JNK and other stress-activated protein kinases, can foster a cellular environment conducive to the activation of ZNF358 through phosphorylation. These chemical activators, by variously influencing the signaling pathways and kinase activities within cells, converge on the common endpoint of ZNF358 phosphorylation and activation.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Isoproterenol Hydrochloride

51-30-9sc-202188
sc-202188A
100 mg
500 mg
$28.00
$38.00
5
(0)

Isoproterenol is a synthetic catecholamine that activates beta-adrenergic receptors, causing an increase in cAMP levels via adenylyl cyclase activation. The rise in cAMP can lead to the activation of PKA, which may then phosphorylate ZNF358, resulting in its functional activation.

8-Bromo-cAMP

76939-46-3sc-201564
sc-201564A
10 mg
50 mg
$126.00
$328.00
30
(1)

8-Bromo-cAMP is a cell-permeable cAMP analog that resists degradation by phosphodiesterases. This chemical can activate PKA, which could phosphorylate ZNF358 and thus lead to its functional activation.

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
$260.00
$350.00
$500.00
34
(1)

IBMX, or 3-Isobutyl-1-methylxanthine, is a non-selective inhibitor of phosphodiesterases, enzymes that degrade cAMP. By preventing cAMP breakdown, IBMX indirectly increases PKA activity, which could then phosphorylate and activate ZNF358.

(−)-Epinephrine

51-43-4sc-205674
sc-205674A
sc-205674B
sc-205674C
sc-205674D
1 g
5 g
10 g
100 g
1 kg
$41.00
$104.00
$201.00
$1774.00
$16500.00
(1)

Epinephrine, also known as adrenaline, interacts with adrenergic receptors and can increase intracellular cAMP levels, leading to the activation of PKA. PKA can then potentially phosphorylate and activate ZNF358.

PGE2

363-24-6sc-201225
sc-201225C
sc-201225A
sc-201225B
1 mg
5 mg
10 mg
50 mg
$57.00
$159.00
$275.00
$678.00
37
(1)

Prostaglandin E2 (PGE2) binds to its G protein-coupled receptor, leading to an increase in cAMP levels and subsequent activation of PKA, which may phosphorylate ZNF358, leading to its activation.

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$99.00
$259.00
36
(2)

Anisomycin is a JNK activator which can also activate stress-activated protein kinases (SAPKs). These kinases can influence the activity of transcription factors and other proteins such as ZNF358 by phosphorylation leading to its functional activation.

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)

Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which can phosphorylate different proteins and could lead to the phosphorylation and activation of ZNF358 as part of a signaling cascade.

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)

Dibutyryl-cAMP is a cAMP analog that is resistant to degradation by cellular enzymes. It activates PKA which could phosphorylate ZNF358, leading to its functional activation.

Rolipram

61413-54-5sc-3563
sc-3563A
5 mg
50 mg
$77.00
$216.00
18
(1)

Rolipram is a selective inhibitor of phosphodiesterase 4 (PDE4), which leads to increased cAMP levels in the cell. The increased cAMP activates PKA which could phosphorylate ZNF358, resulting in its activation.

Zaprinast (M&B 22948)

37762-06-4sc-201206
sc-201206A
25 mg
100 mg
$105.00
$250.00
8
(2)

Zaprinast inhibits phosphodiesterase 5 (PDE5), which can lead to increased cAMP and/or cGMP levels in cells, potentially leading to the activation of PKA and subsequent phosphorylation and activation of ZNF358.