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.
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Nome do Produto | CAS # | Numero de Catalogo | Quantidade | Preco | Uso e aplicacao | NOTAS |
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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 | |
Bloqueia os canais de potássio dependentes da voltagem, afectando potencialmente os canais modulados por KCNG1. | ||||||
Quinidine | 56-54-2 | sc-212614 | 10 g | $102.00 | 3 | |
Bloqueia vários canais de potássio, afectando potencialmente a atividade dos canais relacionados com o KCNG1. | ||||||
Clofilium tosylate | 92953-10-1 | sc-391228 sc-391228A | 25 mg 100 mg | $428.00 $1020.00 | 1 | |
Inibe uma vasta gama de canais de potássio, podendo influenciar os canais modulados por KCNG1. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
Principalmente um bloqueador dos canais de cálcio, mas pode ter efeitos fora do alvo nos canais de potássio. |