Date published: 2026-3-3

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PIA Activators

Chemicals classified as PIA activators encompass a broad spectrum of molecules that interact with varied receptors and enzymes, translating their effects into modulation of the PIA protein. Adenosine, a fundamental nucleoside, engages with its specific receptors to boost adenylate cyclase activity. This elevation in adenylate cyclase can be observed with other chemicals such as Epinephrine and Isoproterenol, both acting on adrenergic receptors. The heightened activity results in amplified cAMP levels, a secondary messenger implicated in numerous cellular pathways.

Further, molecules like PGE2 don't just stop at one pathway. Its interaction with different receptor subtypes enables it to either stimulate adenylate cyclase or activate phospholipase C, showing the intricate web of signaling cascades it can influence. Dopamine, a neurotransmitter, utilizes its D1-like receptors to drive adenylate cyclase activity. In a slightly different approach, Anandamide, through its action on CB1, might inhibit adenylate cyclase. Still, this inhibition can provoke a compensatory response, amplifying the associated pathways. ATP, a molecule fundamental for cellular energy, not only fuels kinases but also modulates purinergic receptors, thereby having a dual effect on cellular pathways. All these chemicals, in their unique manners, can cast a ripple through cellular pathways, reaching proteins like PIA and modulating their activity. This diverse set of chemicals underscores the complexity and interlinked nature of cellular signaling, emphasizing the need to understand each activator's specific role in the broader context of cellular physiology.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Adenosine

58-61-7sc-291838
sc-291838A
sc-291838B
sc-291838C
sc-291838D
sc-291838E
sc-291838F
1 g
5 g
100 g
250 g
1 kg
5 kg
10 kg
$34.00
$48.00
$300.00
$572.00
$1040.00
$2601.00
$4682.00
1
(0)

Nucleoside that binds to adenosine receptors. Activation of certain receptors can stimulate adenylate cyclase leading to increased cAMP levels which can indirectly stimulate proteins in a variety of pathways, including hypothetical PIA.

(−)-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)

Acts on adrenergic receptors. Its binding to β-adrenergic receptors activates adenylate cyclase, potentially leading to the activation of downstream proteins.

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)

Binds to its receptors (EP1-4). Depending on the receptor subtype, it can activate adenylate cyclase or phospholipase C, influencing downstream signaling proteins.

Isoproterenol Hydrochloride

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

A non-selective β-adrenergic receptor agonist. Activates adenylate cyclase, leading to increased cAMP levels and potentially activating proteins in cAMP-dependent pathways.

Histamine, free base

51-45-6sc-204000
sc-204000A
sc-204000B
1 g
5 g
25 g
$94.00
$283.00
$988.00
7
(1)

Binds to its receptors (H1-H4). Through the H2 receptor, histamine can activate adenylate cyclase and elevate cAMP levels, indirectly stimulating proteins in the pathway.

Dobutamine

34368-04-2sc-507555
100 mg
$295.00
(0)

A β1-adrenergic receptor agonist. Increases intracellular cAMP by activating adenylate cyclase, which can activate proteins downstream in related pathways.

Dopamine

51-61-6sc-507336
1 g
$290.00
(0)

Acts on dopamine receptors D1-D5. Through D1-like receptors, it activates adenylate cyclase, potentially influencing downstream proteins.

ATP

56-65-5sc-507511
5 g
$17.00
(0)

Serves as a substrate for several kinases and also acts on purinergic receptors, influencing intracellular calcium levels and adenylate cyclase, potentially activating signaling proteins.

Caffeine

58-08-2sc-202514
sc-202514A
sc-202514B
sc-202514C
sc-202514D
50 g
100 g
250 g
1 kg
5 kg
$33.00
$67.00
$97.00
$192.00
$775.00
13
(1)

Non-selective antagonist of adenosine receptors. Increases cAMP by inhibiting phosphodiesterase, potentially influencing downstream proteins.