Date published: 2026-5-1

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KCNH6 Activators

KCNH6 activators are a class of chemical compounds that specifically target and enhance the activity of the KCNH6 protein, a member of the voltage-gated potassium channel family. These channels are integral membrane proteins that play a critical role in regulating the flow of potassium ions across cell membranes, which is essential for maintaining the cell's membrane potential and controlling various cellular processes, including action potential generation and propagation in excitable tissues. The KCNH6 channel, also known as Ether--go-go-related gene 6 (ERG6), is primarily expressed in the heart and nervous system, where it contributes to the fine-tuning of electrical signaling and the maintenance of cellular excitability. KCNH6 activators bind to specific sites on the channel, promoting its open state and thereby facilitating the flow of potassium ions through the channel.The activation of KCNH6 channels by these activators typically involves the stabilization of the channel in its open conformation, which can influence the duration and frequency of action potentials in excitable cells, such as neurons and cardiac myocytes. This modulation of ion flow can have significant effects on cellular excitability, as potassium channels are key determinants of the repolarization phase of the action potential. By enhancing KCNH6 channel activity, these activators can alter the timing and pattern of electrical signaling within cells, leading to changes in cellular function. Additionally, the interaction between KCNH6 activators and the channel may also affect the channel's interactions with other cellular components, such as scaffolding proteins or other ion channels, thereby influencing broader aspects of cellular signaling and network behavior. Understanding the specific mechanisms by which KCNH6 activators exert their effects is crucial for elucidating the role of this channel in physiological processes and its impact on cellular excitability and function.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

NS 1643

448895-37-2sc-204135
sc-204135A
10 mg
50 mg
$123.00
$473.00
3
(1)

NS 1643, acting as a kcnh6, showcases remarkable reactivity attributed to its unique structural features. The presence of an acyl chloride group enhances its electrophilicity, promoting swift nucleophilic attack and subsequent acylation reactions. Its distinct steric hindrance influences reaction kinetics, allowing for selective pathways in synthetic applications. Furthermore, NS 1643 exhibits notable solubility in polar solvents, facilitating diverse reaction environments and enhancing its utility in organic synthesis.

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 activates adenylate cyclase, leading to increased cAMP levels, which could indirectly modulate the activity of KCNH6 by altering cellular signaling pathways.

Milrinone

78415-72-2sc-201193
sc-201193A
10 mg
50 mg
$165.00
$697.00
7
(0)

Milrinone, a phosphodiesterase inhibitor, increases cAMP levels and might indirectly influence the function of KCNH6.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

EGCG, a component of green tea, has been shown to modulate various ion channels and could have an indirect effect on KCNH6.

Nicorandil

65141-46-0sc-200995
sc-200995B
sc-200995A
sc-200995C
50 mg
100 mg
250 mg
1 g
$57.00
$98.00
$240.00
$500.00
4
(1)

Nicorandil, a potassium channel opener with nitrate-like properties, may indirectly affect the activity of various potassium channels, including KCNH6.

Cilostazol

73963-72-1sc-201182
sc-201182A
10 mg
50 mg
$109.00
$322.00
3
(1)

Cilostazol, a phosphodiesterase inhibitor, raises cAMP levels and could indirectly modulate KCNH6 activity.

Isoproterenol Hydrochloride

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

Isoproterenol, a beta-adrenergic agonist, enhances cAMP levels and could indirectly affect KCNH6 channel activity.