Date published: 2026-5-22

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KCNH1 Inhibitors

KCNH1 inhibitors belong to a specific category of chemical compounds that have garnered interest in the field of molecular biology and ion channel regulation. KCNH1, also known as Ether-à-go-go-related gene 1 (ERG1) or human ether-à-go-go-related gene (hERG), is a protein that functions as a voltage-gated potassium channel. These channels are crucial for the regulation of ion flow across cell membranes, particularly in excitable cells such as neurons and cardiac myocytes. KCNH1 channels play a significant role in controlling the repolarization phase of action potentials, ensuring the proper duration of electrical signals and maintaining the stability of membrane potentials. KCNH1 inhibitors are chemical compounds designed to interact with KCNH1, modulating its ion channel activity and affecting cellular processes reliant on potassium ion flux.

The mechanism of action of KCNH1 inhibitors typically involves their binding to specific sites or domains within the KCNH1 channel protein, often altering its conformation and influencing its ion conductance properties. By doing so, these inhibitors may affect the flow of potassium ions across the cell membrane, leading to changes in cellular excitability, action potential duration, and ion homeostasis. The study of KCNH1 inhibitors is pivotal in advancing our understanding of ion channel physiology, shedding light on the molecular mechanisms that govern membrane potential dynamics in various cell types. Additionally, it contributes to the broader field of electrophysiology and ion channel research, offering valuable tools for investigating the roles of KCNH1 channels in various cellular contexts, including neuronal signaling and cardiac function.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$90.00
$204.00
13
(1)

Triptolide inhibits RNA polymerase II activity, potentially reducing transcription across a range of genes, including KCNH1.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$259.00
41
(3)

Flavopiridol inhibits cyclin-dependent kinases and may downregulate transcription factors, possibly affecting KCNH1 expression.

DRB

53-85-0sc-200581
sc-200581A
sc-200581B
sc-200581C
10 mg
50 mg
100 mg
250 mg
$43.00
$189.00
$316.00
$663.00
6
(1)

DRB is a transcription inhibitor that can suppress RNA polymerase II, potentially decreasing transcription of genes like KCNH1.

Betulinic Acid

472-15-1sc-200132
sc-200132A
25 mg
100 mg
$117.00
$344.00
3
(1)

Betulinic acid may affect gene expression through modulation of transcription factors and signaling pathways, potentially influencing KCNH1.

Caffeic acid phenethyl ester

104594-70-9sc-200800
sc-200800A
sc-200800B
20 mg
100 mg
1 g
$71.00
$296.00
$612.00
19
(1)

This compound can modulate NF-kB and other transcription factors, possibly impacting the expression of genes including KCNH1.

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 alters gene expression via retinoic acid receptors, which could lead to changes in KCNH1 expression levels.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$231.00
$863.00
1
(0)

JQ1 inhibits BET bromodomain proteins, affecting transcription regulation and potentially downregulating genes like KCNH1.

I-CBP112

1640282-31-0sc-507494
25 mg
$400.00
(0)

I-CBP112 is a selective CBP/p300 bromodomain inhibitor, which may influence transcription and thus KCNH1 expression.

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 a tyrosine kinase inhibitor with potential to downregulate signal transduction pathways, indirectly impacting KCNH1 expression.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Rapamycin inhibits mTOR, a key regulator of cell growth and protein synthesis, which could potentially reduce KCNH1 expression.