Date published: 2026-4-24

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KIR3.4 Inhibitors

KIR3.4 inhibitors constitute a distinctive group of chemical entities with a specific affinity for the KIR3.4 ion channel, a subtype of inward-rectifying potassium channels widely distributed in various cell types. These inhibitors exert their effects through a complex interplay with the KIR3.4 channel's structure and function. The KIR3.4 channel, being integral to maintaining cellular membrane and regulating ion flux, plays a pivotal role in numerous physiological processes. KIR3.4 inhibitors interact with binding sites on the channel protein, resulting in conformational changes that intricately modulate its activity. This modulation leads to a decreased permeability of the channel to potassium ions, thereby affecting the cellular membrane and electrical excitability. At a molecular level, the interaction between KIR3.4 inhibitors and the channel involves specific non-covalent interactions, such as hydrogen bonding, hydrophobic interactions, and electrostatic forces. These interactions collectively contribute to the stabilization of the inhibitor-channel complex, influencing the overall conformation and gating properties of the channel. By binding to the channel protein, KIR3.4 inhibitors can alter the opening and closing dynamics of the channel, thereby controlling the flow of potassium ions across the cellular membrane. This fine-tuned regulation holds implications for cellular functions ranging from neurotransmitter release to cardiac rhythm modulation. The specificity of KIR3.4 inhibitors for this particular channel subtype underscores the intricate nature of ion channel pharmacology. The detailed understanding of the molecular mechanisms underlying the interaction between these inhibitors and the KIR3.4 channel provides valuable insights into the broader landscape of ion channel function and regulation. Moreover, these inhibitors serve as invaluable tools for researchers, enabling them to dissect the contributions of KIR3.4 channels to cellular physiology and explore avenues for manipulating ion channel activity for various purposes. Through the lens of chemical biology, KIR3.4 inhibitors offer a window into the fascinating world of ion channels and their role in cellular dynamics.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

PIP2

383907-42-4sc-391159
sc-391159A
100 µg
1 mg
$113.00
$479.00
1
(0)

PIP2 serves as a KIR3.4 inhibitor by selectively binding to the channel's regulatory sites, influencing its conformational state. This interaction disrupts the normal ion conduction pathway, leading to altered channel activity. The compound exhibits unique reaction kinetics, allowing for rapid modulation of channel opening and closing. Additionally, PIP2's structural properties facilitate specific lipid interactions, further impacting membrane dynamics and cellular signaling pathways.

Caffeine

58-08-2sc-202514
sc-202514A
sc-202514B
sc-202514C
sc-202514D
50 g
100 g
250 g
1 kg
5 kg
$33.00
$67.00
$97.00
$192.00
$775.00
13
(1)

Modulates Kir3.4 channels in cardiac tissue through adenosine receptor interaction.

Carbamazepine

298-46-4sc-202518
sc-202518A
1 g
5 g
$33.00
$71.00
5
(0)

Inhibits Kir3.4 channels and affects G-protein signaling pathways, used as an anticonvulsant.