Date published: 2025-9-18

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PRODH2 Activators

PRODH2 Activators are chemicals that indirectly stimulate PRODH2, an enzyme involved in proline metabolism, by influencing upstream cellular processes. Two primary pathways are implicated: the calcium/calmodulin-dependent protein kinase II (CaMKII)-STAT3 pathway and the cAMP-dependent protein kinase (PKA)-CREB pathway.

Chemicals like NMDA, Gabapentin, Verapamil, Nifedipine, A23187, Thapsigargin, Amlodipine, and Diltiazem elevate intracellular calcium levels, triggering the CaMKII-STAT3 pathway. Activated CaMKII phosphorylates STAT3, leading to increased PRODH2 expression. In the PKA-CREB pathway, chemicals like Pentoxifylline and Forskolin raise intracellular cAMP levels. Elevated cAMP activates PKA, which phosphorylates CREB, leading to increased PRODH2 transcription. The diverse structures and properties of these chemicals reflect their various methods of modulating calcium and cAMP levels, which in turn influence PRODH2 expression.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-Methyl-D-Aspartic acid (NMDA)

6384-92-5sc-200458
sc-200458A
50 mg
250 mg
$107.00
$362.00
2
(1)

NMDA is an agonist of the NMDA receptor, which can increase intracellular calcium levels. The influx of calcium can activate the calcium/calmodulin-dependent protein kinase II (CaMKII) pathway. CaMKII phosphorylates Ser727 on STAT3, leading to an increase in PRODH2 expression.

Gabapentin

60142-96-3sc-201481
sc-201481A
sc-201481B
20 mg
100 mg
1 g
$52.00
$92.00
$132.00
7
(1)

Gabapentin, a GABA analogue, increases the intracellular calcium concentration by acting on voltage-gated calcium channels. The rise in calcium levels can activate the CaMKII-STAT3 pathway, indirectly leading to increased PRODH2 expression.

EGTA

67-42-5sc-3593
sc-3593A
sc-3593B
sc-3593C
sc-3593D
1 g
10 g
100 g
250 g
1 kg
$20.00
$62.00
$116.00
$246.00
$799.00
23
(1)

EGTA is a calcium chelator that can reduce intracellular calcium levels. Lowering calcium levels can decrease CaMKII activity, indirectly reducing PRODH2 expression. This implies that an increase in calcium can promote PRODH2 expression.

Verapamil

52-53-9sc-507373
1 g
$367.00
(0)

Verapamil is a calcium channel blocker that can increase intracellular calcium levels under certain conditions. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.

Nifedipine

21829-25-4sc-3589
sc-3589A
1 g
5 g
$58.00
$170.00
15
(1)

Nifedipine is a calcium channel blocker that can increase intracellular calcium levels under certain conditions. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.

A23187

52665-69-7sc-3591
sc-3591B
sc-3591A
sc-3591C
1 mg
5 mg
10 mg
25 mg
$54.00
$128.00
$199.00
$311.00
23
(1)

A23187 is a calcium ionophore that can increase intracellular calcium levels. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$94.00
$349.00
114
(2)

Thapsigargin is an inhibitor of the sarco-/endoplasmic reticulum Ca2+ ATPase (SERCA), causing an increase in intracellular calcium levels. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.

Amlodipine

88150-42-9sc-200195
sc-200195A
100 mg
1 g
$73.00
$163.00
2
(1)

Amlodipine is a calcium channel blocker that can increase intracellular calcium levels under certain conditions. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.

KN-93

139298-40-1sc-202199
1 mg
$178.00
25
(1)

KN-93 is a specific inhibitor of CaMKII. By inhibiting CaMKII, KN-93 reduces the phosphorylation of STAT3, indirectly reducing PRODH2 expression. This implies that activation of CaMKII can promote PRODH2 expression.

Diltiazem

42399-41-7sc-204726
sc-204726A
1 g
5 g
$209.00
$464.00
4
(1)

Diltiazem is a calcium channel blocker that can increase intracellular calcium levels under certain conditions. Increased calcium can activate the CaMKII-STAT3 pathway, leading to upregulation of PRODH2.