ranolazine

ranolazine

美 　英

• 網絡雷諾嗪；嶄新抗心絞痛藥物；雷諾拉嗪

例句

Although several pharmacological activities of ranolazine have been described, the precise way the drug works is not fully understood.

盡管已經說明了雷諾嗪的一些藥理活性，但是該藥的確切作用機制仍未完全了解。

Conclusion Ranolazine can inhibit the fast sodium channel current in rabbit atrial myocytes and indeed has a use-dependent effect.

結論雷諾嗪對兔心房肌細胞快鈉電流有一定的抑制作用，其存在使用依賴性阻滯作用。

The FDA also warned that use of ranolazine is contraindicated in patients with clinically significant hepatic impairment.

美國食品和藥物管理局還警告說，雷諾嗪不適于臨床診斷為肝損害的患者使用。

For patients taking moderate CYP3A inhibitors, ranolazine dosing should be limited to 500 mg twice daily.

患者在服用中度CYP3A抑制劑時，雷諾嗪劑量應限制在500mg內，每天兩次。

METHODS Ranolazine was synthesized by using 2, 6-dimethylaniline and guaiacol as the starting material fellewed by 4 step reactions.

方法以2,6-二甲基苯胺、愈創木酚為原料，經酰化、烴化等4步反應制得雷諾嗪。

Chiral Separation of Ranolazine Hydrochloride Enantiomers by Reversed- phase High Performance Liquid Chromatography

鹽酸雷諾嗪對映體的反相高效液相色譜手性分離

Direct chiral separation of racemic ranolazine by high performance liquid chromatography with chiral stationary phase

高效液相色譜手性固定相法直接拆分外消旋雷諾嗪

Improved synthesis of a novel antianginal agent ranolazine

新型抗心絞痛藥物雷諾嗪的合成工藝改進

Ranolazine Improves Exercise Tolerance in Chronic Angina

雷諾嗪可改善慢性心絞痛患者的運動耐量

Study on Synthesis Process of Ranolazine

雷諾嗪的合成工藝研究

Long-term toxicity of ranolazine in rats

雷諾嗪對大鼠的長期毒性試驗