Date published: 2025-11-1

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CTU2 Activators

The category of CTU2 Activators comprises a range of chemicals that can modulate the function of the CTU2 protein by influencing related signaling pathways or cellular processes. These chemicals primarily operate through two main mechanisms. The first group of activators, including Forskolin, Isoproterenol, IBMX, and Rolipram, functions by increasing the intracellular levels of cyclic AMP (cAMP), which activates Protein Kinase A (PKA). PKA then phosphorylates and activates CTU2. Also included in this category are Bt2cAMP, a direct activator of PKA, and chemicals such as Regorafenib and Staurosporine, which act by inhibiting kinases that negatively regulate the cAMP-PKA signaling pathway, facilitating CTU2 activation.

The second group of activators in this category, including Okadaic acid and Calyculin A, operates by inhibiting protein phosphatases PP1 and PP2A, which are responsible for removing phosphate groups from proteins. By inhibiting these phosphatases, these chemicals increase the overall phosphorylation state of proteins, which can lead to CTU2 activation. LY294002, a PI3K inhibitor, and U0126, a MEK1/2 inhibitor, can also increase cAMP levels indirectly by inhibiting pathways that negatively regulate cAMP-PKA signaling.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Forskolin

66575-29-9sc-3562
sc-3562A
sc-3562B
sc-3562C
sc-3562D
5 mg
50 mg
1 g
2 g
5 g
$76.00
$150.00
$725.00
$1385.00
$2050.00
73
(3)

Forskolin is an activator of adenylate cyclase, which elevates cellular levels of cyclic AMP (cAMP). The increased cAMP levels can activate PKA, a kinase that can phosphorylate and activate CTU2.

Isoproterenol Hydrochloride

51-30-9sc-202188
sc-202188A
100 mg
500 mg
$27.00
$37.00
5
(0)

Isoproterenol is a non-selective beta-adrenergic agonist that stimulates adenylate cyclase, leading to a rise in cAMP and subsequent PKA activation. This sequence of events can result in the phosphorylation and activation of CTU2.

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
$159.00
$315.00
$598.00
34
(1)

IBMX inhibits phosphodiesterases, enzymes that degrade cAMP. By inhibiting these enzymes, IBMX increases cAMP levels, which can activate PKA and result in CTU2 phosphorylation and activation.

Rolipram

61413-54-5sc-3563
sc-3563A
5 mg
50 mg
$75.00
$212.00
18
(1)

Rolipram is a selective PDE4 inhibitor. By inhibiting PDE4, Rolipram increases cAMP levels, which can trigger PKA activation and lead to CTU2 phosphorylation and activation.

Dibutyryl-cAMP

16980-89-5sc-201567
sc-201567A
sc-201567B
sc-201567C
20 mg
100 mg
500 mg
10 g
$45.00
$130.00
$480.00
$4450.00
74
(7)

Bt2cAMP is a membrane-permeable cAMP analog that can activate PKA directly. This PKA activation can lead to the phosphorylation and activation of CTU2.

Regorafenib

755037-03-7sc-477163
sc-477163A
25 mg
50 mg
$320.00
$430.00
3
(0)

Regorafenib is a multi-kinase inhibitor that can indirectly activate CTU2 by inhibiting kinases that negatively regulate cAMP-PKA signaling, thus promoting CTU2 activation.

LY 294002

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

LY294002 is a PI3K inhibitor. It can indirectly increase cAMP levels by inhibiting the PI3K-Akt pathway, a negative regulator of cAMP-PKA signaling, leading to PKA activation and subsequent CTU2 phosphorylation.

Okadaic Acid

78111-17-8sc-3513
sc-3513A
sc-3513B
25 µg
100 µg
1 mg
$285.00
$520.00
$1300.00
78
(4)

Okadaic acid is an inhibitor of protein phosphatases PP1 and PP2A. By inhibiting these phosphatases, okadaic acid can increase the phosphorylation state of proteins, including CTU2.

Calyculin A

101932-71-2sc-24000
sc-24000A
sc-24000B
sc-24000C
10 µg
100 µg
500 µg
1 mg
$160.00
$750.00
$1400.00
$3000.00
59
(3)

Calyculin A is a potent inhibitor of protein phosphatases PP1 and PP2A. By inhibiting these phosphatases, it can increase the phosphorylation state of proteins, potentially activating CTU2.

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$150.00
$388.00
113
(4)

Staurosporine is a broad-spectrum kinase inhibitor that can indirectly activate CTU2 by inhibiting kinases that negatively regulate cAMP-PKA signaling.