Date published: 2026-5-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

Olr286 Activators

Chemical activators of Olr286 can engage various signaling pathways to achieve functional upregulation. Forskolin directly stimulates adenylyl cyclase, which catalyzes the conversion of ATP to cyclic AMP (cAMP). Elevated cAMP levels in turn activate protein kinase A (PKA), an enzyme capable of phosphorylating multiple targets, leading to the activation of Olr286. Similarly, IBMX acts as a non-specific inhibitor of phosphodiesterases, enzymes responsible for the breakdown of cAMP, resulting in the accumulation of cAMP within the cell and subsequent activation of PKA, which may enhance the activity of Olr286. Isoproterenol, a synthetic agonist for beta-adrenergic receptors, and Epinephrine, which stimulates both alpha and beta-adrenergic receptors, both lead to increased cAMP production. The rise in cAMP levels activates PKA, subsequently contributing to the activation of Olr286.

Adenosine, through the activation of A2 adenosine receptors, also leads to an increase in cAMP levels, fostering a cellular environment that promotes PKA activity and Olr286 activation. Prostaglandin E2 interacts with its EP receptors to stimulate cAMP production, while Glucagon, via its receptor, activates adenylyl cyclase, both resulting in PKA activation and potential Olr286 activation. PACAP, by binding to its receptors, and Histamine, through H2 receptors, both lead to elevated cAMP concentrations, which activate PKA and in turn, may activate Olr286. Cholera toxin permanently activates the Gs alpha subunit, resulting in sustained adenylyl cyclase activity and increased cAMP levels, which leads to prolonged PKA activation and consequent Olr286 activation. Vardenafil, by inhibiting phosphodiesterase type 5, prevents the breakdown of cAMP, thus maintaining an activated state of PKA, which can then contribute to the activation of Olr286. Each chemical, by elevating cAMP levels or inhibiting its degradation, creates a cascade of events that culminates in the activation of PKA, thereby facilitating the activation of Olr286.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

IBMX

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

Non-specific inhibitor of phosphodiesterases, increases cAMP levels, enhancing PKA activity and Olr286 activation.

Isoproterenol Hydrochloride

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

Agonist at beta-adrenergic receptors, increases cAMP production, indirectly leading to Olr286 activation via PKA.

(−)-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)

Stimulates alpha and beta-adrenergic receptors, boosting cAMP and activating PKA, which can then activate Olr286.

Dopamine

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

Binds to D1-like dopamine receptors, increasing cAMP levels and PKA activity, potentially activating Olr286.

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)

Activates A2 adenosine receptors, increasing cAMP levels which can lead to PKA-mediated Olr286 activation.

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)

Interacts with EP receptors, stimulating cAMP production, which activates PKA and subsequently Olr286.

PACAP(6-38)

137061-48-4sc-391136
sc-391136A
500 µg
1 mg
$540.00
$932.00
(0)

Binds to its receptors, increasing cAMP and activating PKA, which may lead to activation of Olr286.

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)

Through H2 receptors, elevates cAMP levels, enhancing PKA activity and possibly Olr286 activation.

Vardenafil

224785-90-4sc-362054
sc-362054A
sc-362054B
100 mg
1 g
50 g
$526.00
$735.00
$16653.00
7
(1)

Inhibits phosphodiesterase type 5, increasing cAMP concentration in cells, which can lead to Olr286 activation through PKA.