Date published: 2026-4-24

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Neuro D2 Activators

Neuro D2 activators refer to a class of chemical compounds that are designed to selectively interact with the dopamine D2 receptor, a G protein-coupled receptor (GPCR) found in the brain. The dopamine D2 receptor is one of five subtypes in the dopamine receptor family and plays a critical role in modulating neurotransmission within the central nervous system. Dopamine itself is a neurotransmitter that is involved in a wide range of neural processes, including motivation, pleasure, cognition, memory, learning, and fine motor control. The binding of neuro D2 activators to these receptors triggers a cascade of intracellular events by mimicking the action of dopamine, which can lead to changes in neuron activity and neurotransmitter release.

The chemical structure of neuro D2 activators is typically characterized by their ability to fit into the binding site of the D2 receptor with high specificity. This means that the activators are often designed to have structural features that closely resemble those of the natural ligand, dopamine, to ensure they interact with the receptor in a similar manner. The specificity is crucial because it determines the selectivity of the compound for the D2 receptor over other types of dopamine receptors, as well as other GPCRs, which minimizes off-target effects. The precise interaction between neuro D2 activators and the D2 receptor involves a combination of hydrogen bonds, hydrophobic interactions, and van der Waals forces, which together contribute to the stability and efficacy of the binding. The design and development of these compounds involve a deep understanding of the receptor's structure and the dynamic processes that govern ligand-receptor interactions within the complex environment of the brain.

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
$78.00
$153.00
$740.00
$1413.00
$2091.00
73
(3)

Forskolin directly stimulates adenylyl cyclase, resulting in increased production of cyclic AMP (cAMP) in cells. Elevated cAMP levels enhance the PKA signaling pathway, which phosphorylates CREB, potentially increasing transcriptional activity of Neuro D2.

Rolipram

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

Rolipram inhibits phosphodiesterase 4 (PDE4), preventing the breakdown of cAMP. The consequent rise in cAMP levels can enhance PKA activity, leading to activation of CREB, which may result in upregulated expression and activity of Neuro D2.

Ionomycin

56092-82-1sc-3592
sc-3592A
1 mg
5 mg
$78.00
$270.00
80
(4)

Ionomycin is a calcium ionophore that increases intracellular calcium levels. The rise in calcium can activate CaMKII, which may enhance CREB phosphorylation, thus potentially upregulating Neuro D2 through increased transcriptional activity.

K-252a

99533-80-9sc-200517
sc-200517B
sc-200517A
100 µg
500 µg
1 mg
$129.00
$214.00
$498.00
19
(2)

K-252a inhibits Trk receptor tyrosine kinases, which could lead to a compensatory upregulation in neurotrophic factor signaling, potentially enhancing the activity of Neuro D2 as the nervous system works to maintain neurotrophic support.

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 cyclic-AMP (dbcAMP) is a cell-permeable analog of cAMP that can directly activate PKA. The activation of PKA can enhance CREB phosphorylation, leading to a potential increase in Neuro D2 expression and activity.

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 binds to retinoic acid receptors (RARs), which can modulate gene expression. This binding can lead to differentiation of neurons and may influence the expression of Neuro D2 by altering the transcriptional landscape during development.

Anisomycin

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

Anisomycin is a protein synthesis inhibitor that, paradoxically, can activate stress response pathways such as the MAPK/ERK pathway. This activation can lead to enhanced neuronal plasticity and potentially upregulate Neuro D2 through stress response gene networks.