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Fimasartan
总货号: MB3599
货号 规格 库存 发货时间
5MG [¥800.00] :¥800.00
15
现货
25MG [¥2000.00] :¥2000.00
15
现货
数量
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Fimasartan
分子式:C27H31N7OS分子量:501.65

简介: Fimasartan是一种非肽段的angiotensin II receptor拮抗剂,与AT1受体非竞争性地结合。用于高血压和心力衰竭的治疗中。 
中文名:非马沙坦 
物理性状及指标: 
外观:……………………粉末 
溶解性:…………………H2O :Insoluble;Ethanol:24 mg/mL (47.84 mM);DMSO: 100 mg/mL (199.34 mM) 
含量:……………………>98% 
储存温度:-20℃,避光防潮密闭干燥

生物活性

描述

Fimasartan是一种非肽段的angiotensin II receptor拮抗剂,与AT1受体非竞争性地结合。用于高血压和心力衰竭的治疗中。

IC50 & Target

AT1 receptor 

 
 

体外

Fimasartan is a selective AT1 receptor antagonist. The concentration that inhibits the binding of [125I]Ang II to the AT1 receptor from rat adrenal cortex by 50% (IC50) is 0.13 nM. Fimasartan shows superior inhibitory activity in the contraction of isolated rabbit thoracic aorta compared to other ARBs such as losartan and candesartan. Fimasartan potently attenuates myocardial apoptotic death in reperfused rat heart and H9c2 cells. Fimasartan could attenuate mitochondrial damage which is associated with minimizing the reduction in Bcl-2 and connected with the reduction in p53 and activation of Akt and GSK-3β, and inhibiting mitochondrial Ca2+ overload by suppressing the ICa,L and MCU.

体内

In various animal models including renal hypertensive rats, spontaneously hypertensive rats and Beagle dogs, fimasartan effectively reduces blood pressure in a dose-dependent manner following single or repeated oral and intravenous administration. Fimasartan does not affect general behavior, respiratory rate or tidal volume in experimental animals, and shows no adverse findings in the human ether-a-go-go-related gene (hERG) test or monkey telemetry study. A number of general toxicity, carcinogenic toxicity, genetic toxicity, and developmental toxicity studies given either orally or intravenously in various species including mice, rats, monkeys and dogs are conducted and these preclinical results demonstrate the safety and tolerability of fimasartan for long-term clinical use and offer sufficient safety margins to support the expected human therapeutic dose. Fimasartan is rapidly absorbed following oral administration with the time to peak plasma concentration (Tmax) ranging 0.5-3 h and the terminal half-life (t1/2) being 5-16 h at doses of 20 to 480 mg in healthy subjects. Similar results are obtained in patients with hypertension, i.e., Tmax ranges 0.5-1.3 h and t1/2 is 7-10 h following fimasartan administration at doses 20-180 mg in the subsequent phase II study. The urinary excretion of fimasartan is low, with the overall urinary excretion of unchanged drug over the first 24 h after dosing being less than 3% of the administered dose. Fimasartan undergoes nonrenal elimination with minimal metabolism. Fimasartan treatment before myocardial ischemia significantly attenuates reperfusion .injury and apoptotic changes, possibly by suppressing mitochondrial damage during reperfusion In various preclinical studies, including aortic balloon injury, myocardial infarct ischemia/reperfusion, doxorubicin cardiotoxicity, and ischemic stroke models, fimasartan shows anti-inflammatory and organ-protecting effects.

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储液配置及储存: 按表中溶解性配置;如溶解困难,可以通过快速搅拌,超声或温和加热(在45-60°C下水浴)。液体稳定性报道的很少,建议现配现用,如需储存,建议:-20℃1-3月;-80℃ 3-6月。

1 mg

5 mg

10 mg

1 mM

1.9934 mL

9.9671 mL

19.9342 mL

5 mM

0.3987 mL

1.9934 mL

3.9868 mL

10 mM

0.1993 mL

0.9967 mL

1.9934 mL

50 mM

0.0399 mL

0.1993 mL

0.3987 mL

【注意 
我司产品为非无菌包装,若用于细胞培养,请提前做预处理,除去热原细菌,否则会导致染菌。

部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,以上数据仅供参考交流研究之用。

我司所售出产品仅供于科研研究用途(非临床科研研究),每次销售产品行为都适用于我司网上所列明的通用销售条款。


CAS 号:247257-48-3
英文名字:非马沙坦
质量标准:>98%,BR
分子式:C27H31N7OS
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