Date published: 2025-9-11

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KCNG2 抑制因子

KCNG2 inhibitors are a class of chemical compounds that selectively inhibit the KCNG2 protein, a subunit of the voltage-gated potassium channel family. KCNG2, also known as Kv6.2, is part of a diverse group of ion channels that regulate potassium ion flux across cell membranes, contributing to the maintenance of the resting membrane potential and shaping the action potential in excitable cells. As a modulatory subunit, KCNG2 does not form functional channels by itself but co-assembles with other Kv subunits, particularly those from the Kv2 family, to form heteromeric channels with distinct biophysical and pharmacological properties. Inhibitors of KCNG2 are therefore key tools in understanding the specific contributions of this subunit to the overall function of voltage-gated potassium channels. The modulation of these channels by KCNG2 inhibitors can provide insights into the physiological roles of KCNG2-containing channels in various cellular processes, including electrical signaling, cell proliferation, and apoptosis.

The design and development of KCNG2 inhibitors often involve high-throughput screening techniques and structure-activity relationship (SAR) studies to identify compounds that specifically target the KCNG2 subunit without affecting other potassium channels. This specificity is crucial, as it allows researchers to delineate the role of KCNG2 in cellular electrophysiology and its impact on cell behavior in both normal and pathological states. Studies using KCNG2 inhibitors have demonstrated that these compounds can modulate neuronal excitability and synaptic transmission, making them valuable tools for neurophysiological research. Additionally, these inhibitors can be used to investigate the contributions of KCNG2-containing channels to the electrical properties of other excitable cells, such as cardiac and smooth muscle cells. By selectively blocking KCNG2, researchers can better understand the complex network of potassium channels and their regulation, ultimately contributing to a more comprehensive understanding of cellular excitability and signaling.

関連項目

产品名称CAS #产品编号数量价格应用排名

4-Aminopyridine

504-24-5sc-202421
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sc-202421A
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$37.00
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3
(2)

阻断电压门控钾通道,可能影响受 KCNG2 调节的通道。

Quinidine

56-54-2sc-212614
10 g
$102.00
3
(1)

阻断各种钾通道,可能影响 KCNG2 相关通道的活性。

Clofilium tosylate

92953-10-1sc-391228
sc-391228A
25 mg
100 mg
$428.00
$1020.00
1
(0)

抑制一系列钾通道,可能影响 KCNG2 调节的通道。

Verapamil

52-53-9sc-507373
1 g
$367.00
(0)

主要是一种钙通道阻滞剂,但可对钾通道产生脱靶效应。