Ranolazine CAS NO.95635-55-5

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Category:Active Pharmaceutical Ingredients   MOQ:100KG  Shipped directly from China

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Introduction

Catalog ID80017137

CAS NO.95635-55-5

Purity 95%

MDL NumberMFCD00864690

EINEC Molecular Formula C24H33N3O4

Molecular Weight 427.5365

Aspect Details
Mechanism of Action Ranolazine is a late sodium channel blocker that inhibits the late sodium current (INa,late) in cardiac muscle cells. This action prevents calcium overload, reduces left ventricular wall tension, and increases coronary blood flow, leading to relief of angina. It also stabilizes the myocardial cell membrane, contributing to its anti-arrhythmic effects.
Clinical Uses Ranolazine is primarily used for the treatment of chronic stable angina. It is also being explored for its potential benefits in managing ischemic heart disease, particularly in patients with diabetes mellitus, and for preventing post-cardioversion and post-CABG atrial fibrillation.
Dosage Forms Available as extended-release tablets in doses of 500 mg and 1000 mg. Typical dosing is 500–1000 mg twice daily.
Storage Conditions Should be stored at room temperature, between 68°F to 77°F (20°C to 25°C), and can be exposed to temperatures between 59°F to 86°F (15°C to 30°C) for shorter periods.
Side Effects Common side effects include dizziness, headache, constipation, nausea, and fatigue. More serious adverse effects may include QT prolongation, renal impairment, and allergic reactions.
Drug Interactions Ranolazine is metabolized primarily by CYP3A4. Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin) and inducers (e.g., rifampin, St. John’s wort) can significantly alter ranolazine levels. Co-administration with metformin requires careful monitoring of blood glucose levels.
Special Considerations Caution is advised in patients with a history of long QT syndrome or renal impairment. Ranolazine is contraindicated in patients with hepatic cirrhosis and those allergic to the drug.
Monitoring Regular monitoring of the QT interval is recommended, especially when used with other QT-prolonging drugs. Patients should also be monitored for signs of renal impairment and neurologic adverse effects.

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