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Lisinopril

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纯度: 99.34%

货号 T21418Cas号 76547-98-3

别名 赖诺普利, Zestril, Prinivil, Lisipril, Linopril

Lisinopril (Prinivil) 是一种血管紧张素转化酶抑制剂,能够作用于高血压,充血性心力衰竭和心脏病等。

Lisinopril

Lisinopril

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Rating icon 还可以

纯度: 99.34%

货号 T21418 别名 赖诺普利, Zestril, Prinivil, Lisipril, LinoprilCas号 76547-98-3

Lisinopril (Prinivil) 是一种血管紧张素转化酶抑制剂,能够作用于高血压,充血性心力衰竭和心脏病等。

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100 mg
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200 mg
¥ 215
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500 mg
¥ 418
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产品介绍


Lisinopril AI Summary
Lisinopril exhibits potent inhibitory activity against the angiotensin-converting enzyme (ACE) with varying IC50 values measured in different assays, prominently including 1.2 nM and 0.1 nM in human serum assays. Its effectiveness in inhibiting ACE suggests potential uses in regulating blood pressure and cardiovascular function. Additionally, Lisinopril displays selectivity towards the ACE C domain over the N domain, with respective Ki values of 51.0 nM and 131.5 nM. Beyond ACE inhibition, this compound has demonstrated antiviral activity against SARS-CoV-2, although with moderate efficacy, and shows specific binding affinities to metal ions such as zinc and cupric. It has been assessed for various pharmacokinetic properties, including a half-life of 42 hours, a volume of distribution at 0.89 L.kg-1, and moderate total clearance and renal clearance each at 1.2 mL.min-1.kg-1. The compound exhibits low oral bioavailability (25.0%) and significant gut-wall elimination escape (Fg = 0.89). Additionally, it is involved in drug-related liver injury with a DILI severity class of 3.0, as evidenced by elevated liver enzyme levels. Lastly, Lisinopril shows inhibitory effects on rabbit and human liver transporters and modest cytotoxicity against human cell lines..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Lisinopril (Prinivil), the angiotensin-converting enzyme (ACE) inhibitor, is used primarily in the treatment of high heart failure, blood pressure, and heart attacks. It is also used for preventing eye and kidney complications in people with diabetes.
别名赖诺普利, Zestril, Prinivil, Lisipril, Linopril
化学信息
分子量405.49
分子式C21H31N3O5
CAS No.76547-98-3
SmilesC([C@@H](N[C@@H](CCC1=CC=CC=C1)C(O)=O)CCCCN)(=O)N2[C@H](C(O)=O)CCC2
密度1.251 g/cm3 (Predicted)
颜色White
物理性状Solid
储存&溶解度
存储store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: < 1 mg/mL (insoluble or slightly soluble)
H2O: 11.1 mg/mL (27.37 mM), Sonication is recommended.
溶液配制表
H2O
1mg5mg10mg50mg
1 mM2.4662 mL12.3308 mL24.6615 mL123.3076 mL
5 mM0.4932 mL2.4662 mL4.9323 mL24.6615 mL
10 mM0.2466 mL1.2331 mL2.4662 mL12.3308 mL
20 mM0.1233 mL0.6165 mL1.2331 mL6.1654 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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