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.
제품명 | CAS # | 카탈로그 번호 | 수량 | 가격 | 引用 | RATING |
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4-Aminopyridine | 504-24-5 | sc-202421 sc-202421B sc-202421A | 25 g 1 kg 100 g | $37.00 $1132.00 $120.00 | 3 | |
전압 게이트 칼륨 채널을 차단하여 KCNG1에 의해 변조되는 채널에 잠재적으로 영향을 줄 수 있습니다. | ||||||
Quinidine | 56-54-2 | sc-212614 | 10 g | $102.00 | 3 | |
다양한 칼륨 채널을 차단하여 잠재적으로 KCNG1 관련 채널 활동에 영향을 미칩니다. | ||||||
Clofilium tosylate | 92953-10-1 | sc-391228 sc-391228A | 25 mg 100 mg | $428.00 $1020.00 | 1 | |
광범위한 칼륨 채널을 억제하고 KCNG1 변조 채널에 영향을 줄 수 있습니다. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
주로 칼슘 채널 차단제이지만 칼륨 채널에 표적을 벗어난 영향을 미칠 수 있습니다. |