Date published: 2025-9-16

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FXYD4 Inhibitors

FXYD4 inhibitors comprise a diverse range of chemicals that indirectly modulate the function and activity of FXYD4, a regulatory protein of the Na+/K+-ATPase pump. These inhibitors primarily function by altering the activity of the Na+/K+-ATPase pump, ionic homeostasis, or the signaling pathways related to FXYD4's regulatory role. Compounds like Ouabain and Digoxin, cardiac glycosides that inhibit the Na+/K+-ATPase pump, can indirectly affect FXYD4's modulation of the pump. Similarly, ACE inhibitors like Captopril and aldosterone antagonists like Spironolactone may influence FXYD4's activity by affecting the electrolyte balance and Na+/K+-ATPase pump function. Other inhibitors, such as potassium-sparing diuretics like Amiloride and Triamterene, modulate sodium and potassium balance, impacting FXYD4's regulatory role. Calcium channel blockers, including Verapamil and Nifedipine, indirectly influence Na+/K+-ATPase activity and consequently FXYD4 function by modulating calcium signaling. Magnesium Sulphate, vital for ATPase function, and Dexamethasone, a glucocorticoid, can also modulate Na+/K+-ATPase activity, thus affecting FXYD4. Furthermore, compounds like Prostaglandin E2 and Epinephrine, which modulate various physiological processes including ion transport, potentially impact FXYD4-regulated pathways.

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