Date published: 2026-5-1

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TRESK Activators

TRESK activators are a category of chemical compounds that modulate the activity of the TRESK protein, which is a member of the two-pore domain potassium channel family (K2P). TRESK, also known as KCNK18, is characterized by its ability to control the flow of potassium ions across the cellular membrane, contributing to the regulation of the membrane potential in certain cells. The activation of TRESK generally leads to the hyperpolarization of cells, making them less excitable. This is a critical function in the modulation of neuronal excitability and has implications for the understanding of sensory perception and signal transduction. The activation of TRESK by these compounds can occur through various mechanisms. Direct activators may bind to specific sites on the TRESK channel, inducing a conformational change that allows potassium ions to flow more freely through the channel. This binding may stabilize the open state of the channel or shift the channel's gating equilibrium towards the open state, enhancing its activity.

Indirect activators may influence the activity of TRESK by altering the intracellular signaling pathways that modulate the channel's function. This could include the activation of various kinases or phosphatases that phosphorylate or dephosphorylate the channel, respectively, leading to changes in TRESK activity. Additionally, secondary messengers or changes in intracellular ion concentrations could affect the channel's gating properties or expression levels, ultimately leading to increased TRESK activity. In research settings, TRESK activators are employed to study the physiological role of TRESK channels in cellular signaling and the maintenance of resting membrane potential. By selectively enhancing the activity of TRESK, researchers can investigate its contribution to the modulation of neuronal excitability and to the cellular responses to changes in the extracellular environment.

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 is a direct activator of adenylate cyclase, which increases the intracellular levels of cAMP. TRESK channels are known to be activated by an increase in intracellular cAMP levels, thus forskolin indirectly activates TRESK by increasing cAMP levels.

Genistein

446-72-0sc-3515
sc-3515A
sc-3515B
sc-3515C
sc-3515D
sc-3515E
sc-3515F
100 mg
500 mg
1 g
5 g
10 g
25 g
100 g
$45.00
$164.00
$200.00
$402.00
$575.00
$981.00
$2031.00
46
(1)

Genistein is an activator of protein tyrosine kinase (PTK). Activation of PTK can lead to the phosphorylation of TRESK, which enhances its activity. Thus, genistein can indirectly activate TRESK via PTK activation.

8-Bromo-cAMP

76939-46-3sc-201564
sc-201564A
10 mg
50 mg
$126.00
$328.00
30
(1)

8-Br-cAMP is a cell-permeable cAMP analog. It increases intracellular cAMP levels, which can activate TRESK channels. Therefore, 8-Br-cAMP can indirectly activate TRESK by increasing intracellular cAMP levels.

Capsaicin

404-86-4sc-3577
sc-3577C
sc-3577D
sc-3577A
50 mg
250 mg
500 mg
1 g
$96.00
$160.00
$240.00
$405.00
26
(1)

Capsaicin is an activator of TRPV1 channels. Activation of TRPV1 can lead to a cellular response that results in the activation of TRESK channels. Thus, capsaicin might indirectly activate TRESK via TRPV1 activation.

Charybdotoxin

95751-30-7sc-200979
100 µg
$401.00
9
(0)

Charybdotoxin is a potent inhibitor of large conductance calcium-activated potassium (BK) channels. Inhibition of BK channels can lead to changes in membrane potential that may indirectly activate TRESK.

Diazoxide

364-98-7sc-200980
1 g
$300.00
5
(1)

Diazoxide opens ATP-sensitive potassium channels, which can induce hyperpolarization and indirectly activate TRESK channels.

Glyburide (Glibenclamide)

10238-21-8sc-200982
sc-200982A
sc-200982D
sc-200982B
sc-200982C
1 g
5 g
25 g
100 g
500 g
$46.00
$61.00
$117.00
$173.00
$530.00
36
(1)

Glibenclamide is an inhibitor of ATP-sensitive potassium channels. Its inhibition can lead to membrane depolarization which may indirectly activate TRESK channels.

Pregnenolone sulfate sodium salt

1852-38-6sc-301609
50 mg
$99.00
2
(1)

Pregnenolone sulfate is an endogenous neurosteroid that has been shown to directly activate TRESK channels, enhancing their activity.