KCNH7 Inhibitors encompasses a group of compounds that specifically target KCNH7 channels, which are voltage-gated potassium channels expressed in various tissues, including the heart and neurons. KCNH7 channels play a crucial role in regulating cellular excitability by controlling the movement of potassium ions across cell membranes. Inhibition of these channels could potentially influence electrical signaling and cellular responses. The development of KCNH7 inhibitors involves the exploration of compounds that can selectively interact with these channels, modulating their function and altering ion flow.
KCNH7 inhibitors are characterized by their ability to bind to specific sites on KCNH7 channels, thus altering the channel's conformation and subsequently affecting the movement of potassium ions. These inhibitors may act by impeding ion movement through the channel pore or by affecting the voltage-dependent gating mechanism that controls channel opening and closing. Chemical compounds within this class can vary widely in their structural properties and mechanisms of action. By inhibiting KCNH7 channels, these compounds have the potential to impact electrical excitability in various tissues, potentially influencing physiological processes and signaling cascades that involve these channels. KCNH7 Inhibitors constitute a diverse class of compounds that interact with KCNH7 channels, modulating their ion-conducting properties and potentially affecting cellular excitability. The development and study of these inhibitors provide insights into the functional role of KCNH7 channels in various physiological contexts. It's worth noting that further research is essential to understand the specific mechanisms by which these inhibitors interact with KCNH7 channels and the broader implications of their modulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cisapride | 81098-60-4 | sc-203894 sc-203894A | 10 mg 50 mg | $119.00 $480.00 | 1 | |
Originally developed as a prokinetic agent for gastrointestinal disorders, cisapride also inhibits KCNH7 channels. It has been used to study the channel's role in cardiac repolarization. | ||||||
Terfenadine | 50679-08-8 | sc-208421A sc-208421B sc-208421 | 500 mg 1 g 5 g | $44.00 $71.00 $120.00 | ||
Terfenadine was an antihistamine with KCNH7 inhibitory properties that faced restrictions due to potential cardiac effects. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $69.00 | 2 | |
Chloroquine has been investigated for its potential to inhibit KCNH7 channels, which might be relevant to its cardiotoxicity profile. | ||||||
Haloperidol | 52-86-8 | sc-507512 | 5 g | $190.00 | ||
An antipsychotic agent in research, haloperidol, has been suggested to inhibit KCNH7 channels, potentially contributing to its effects on neurotransmission. | ||||||
Bepridil | 64706-54-3 | sc-507400 | 100 mg | $1620.00 | ||
Originally an antianginal agent, bepridil also modulates ion channels, including KCNH7, and has been associated with cardiac effects. | ||||||
Fluoxetine | 54910-89-3 | sc-279166 | 500 mg | $318.00 | 9 | |
This selective serotonin reuptake inhibitor (SSRI) has been suggested to affect KCNH7 channels, potentially contributing to its neurological effects. | ||||||
Amiodarone | 1951-25-3 | sc-480089 | 5 g | $318.00 | ||
Primarily used for cardiac arrhythmias, amiodarone affects multiple ion channels, including KCNH7, which could contribute to its antiarrhythmic properties. | ||||||
Ketoconazole | 65277-42-1 | sc-200496 sc-200496A | 50 mg 500 mg | $63.00 $265.00 | 21 | |
An antifungal agent, ketoconazole has been investigated for its inhibitory effects on various ion channels, including KCNH7. | ||||||