KCNG1 inhibitors are a class of chemical compounds that target and modulate the function of the KCNG1 channel, also known as the Kv6.1 subunit. KCNG1 is a member of the voltage-gated potassium (Kv) channel family, specifically belonging to the Kv6 subfamily. These channels are integral membrane proteins that facilitate the selective flow of potassium ions across the cell membrane, which is crucial for maintaining the membrane potential and regulating cellular excitability. KCNG1 itself does not form functional channels when expressed alone; instead, it assembles with other Kv2 channel subunits to modulate their properties. The inhibition of KCNG1 has the potential to alter the biophysical properties of these heteromeric channels, affecting their voltage sensitivity, gating kinetics, and ion conduction properties. This makes KCNG1 inhibitors an important tool in understanding the nuanced roles that these auxiliary subunits play in cellular physiology, particularly in excitable cells such as neurons and muscle cells.
The study of KCNG1 inhibitors involves examining their chemical structure, binding affinity, and mechanisms of action. Inhibitors can be designed to specifically target the KCNG1 subunit within the Kv channel complex, allowing researchers to dissect the contributions of KCNG1 to overall channel function. This specificity is achieved through the development of molecules that interact uniquely with the protein domains of KCNG1, potentially binding to allosteric sites or interacting directly with the voltage-sensing or pore-forming regions of the Kv channel complex. Researchers utilize various techniques, such as electrophysiology, molecular modeling, and high-throughput screening, to identify and characterize these inhibitors. By exploring the structure-activity relationships of these compounds, scientists can gain insight into the fundamental processes governing ion channel modulation and the potential for using these insights to develop new chemical tools for probing cellular signaling pathways. Understanding how KCNG1 inhibitors interact with their targets at a molecular level is essential for advancing knowledge in cellular electrophysiology and the broader field of ion channel research.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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4-Aminopyridine | 504-24-5 | sc-202421 sc-202421B sc-202421A | 25 g 1 kg 100 g | ¥417.00 ¥12771.00 ¥1354.00 | 3 | |
阻断电压门控钾通道,可能影响受 KCNG1 调节的通道。 | ||||||
Quinidine | 56-54-2 | sc-212614 | 10 g | ¥1151.00 | 3 | |
阻断各种钾通道,可能影响 KCNG1 相关通道的活性。 | ||||||
Clofilium tosylate | 92953-10-1 | sc-391228 sc-391228A | 25 mg 100 mg | ¥4829.00 ¥11508.00 | 1 | |
抑制多种钾通道,可能影响 KCNG1 调制通道。 | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | ¥4140.00 | ||
主要是一种钙通道阻滞剂,但可对钾通道产生脱靶效应。 |