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Nicardipine

产品号 DB00622 公司名称 DrugBank
CAS号 55985-32-5 公司网站 http://www.ualberta.ca/
分子式 C26H29N3O6 电 话 (780) 492-3111
分子量 479.52496 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 504

产品价格信息

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产品别名

标题
Nicardipine
IUPAC标准名
3-{2-[benzyl(methyl)amino]ethyl} 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
IUPAC传统名
nicardipine
商标名
Cardene IV
Cardene SR
Cardene
别名
Nicardipino [INN-Spanish]
Nicardipine HCl
Nicardipinum [INN-Latin]

产品登记号

PubChem CID 4474
CAS号 55985-32-5
PubChem SID 46504482

产品性质

疏水性(logP) 3.6
溶解度 2.2 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A potent calcium channel blockader with marked vasodilator action. It has antihypertensive properties and is effective in the treatment of angina and coronary spasms without showing cardiodepressant effects. It has also been used in the treatment of asthma and enhances the action of specific antineoplastic agents. [PubChem]
Indication Used for the management of patients with chronic stable angina and for the treatment of hypertension.
Pharmacology Nicardipine, a dihydropyridine calcium-channel blocker, is used alone or with an angiotensin-converting enzyme inhibitor, to treat hypertension, chronic stable angina pectoris, and Prinzmetal's variant angina. Nicardipine is similar to other peripheral vasodilators. Nicardipine inhibits the influx of extra cellular calcium across the myocardial and vascular smooth muscle cell membranes possibly by deforming the channel, inhibiting ion-control gating mechanisms, and/or interfering with the release of calcium from the sarcoplasmic reticulum. The decrease in intracellular calcium inhibits the contractile processes of the myocardial smooth muscle cells, causing dilation of the coronary and systemic arteries, increased oxygen delivery to the myocardial tissue, decreased total peripheral resistance, decreased systemic blood pressure, and decreased afterload.
Toxicity Oral LD50 Rat = 184 mg/kg, Oral LD50 Mouse = 322 mg/kg
Affected Organisms
Humans and other mammals
Biotransformation Nicardipine HCl is metabolized extensively by the liver.
Absorption While nicardipine is completely absorbed, it is subject to saturable first pass metabolism and the systemic bioavailability is about 35% following a 30 mg oral dose at steady state.
Half Life 8.6 hours
Protein Binding >95%
Elimination Nicardipine has been shown to be rapidly and extensively metabolized by the liver.
Distribution * 8.3 L/kg
Clearance * 0.4 L/hr?kg [Following infusion]
External Links
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RxList
Drugs.com

参考文献