货号:A117961
同义名:
赖诺普利二水合物
/ MK-521 dihydrate; Lisinopril(dihydrate)
Lisinopril Dihydrate 是一种血管紧张素转化酶抑制剂,适用于高血压、心力衰竭及心血管功能研究。


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| 描述 | Lisinopri dihydrate is angiotensin-converting enzyme inhibitor, used in treatment of hypertension, congestive heart failure, and heart attacks. Lisinopril is the only ACE inhibitor that exhibits a linear dose-response curve. Lisinopril may be used to treat hypertension and symptomatic congestive heart failure, to improve survival in certain individuals following myocardial infarction, and to prevent progression of renal disease in hypertensive patients with diabetes mellitus and microalbuminuria or overt nephropathy[3]. In all concentrations (25, 75 and 250 mg/l drinking water), lisinopril significantly increased PRA (plasma renin) and decreased ACE activities. Arterial blood pressure was decreased only in the group receiving high lisinopril concentration (Controls 119+/-10.27, Ld3 98+/-5.4 mm Hg)[4]. Systolic blood pressure (SBP) was normal in Wistar rats, SHR (spontaneously hypertensive rats) expressed hypertension and lisinopril normalized the SBP. Lisinopril normalized the increase in SBP and partly reversed the alterations of anxiety-like behaviour in SHR[5]. |
| Concentration | Treated Time | Description | References | |
| Peritoneal-derived macrophages | 1 μM | 24 h | To evaluate the effect of Lisinopril on the phagocytosis of Aβ42 fibrils by wild-type macrophages. Results showed that Lisinopril significantly reduced the phagocytic ability of wild-type macrophages for Aβ42 fibrils. | Brain. 2020 Jan 1;143(1):336-358. |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | Duchenne muscular dystrophy model | Drinking water | 10 mg/kg/day lisinopril and 37.5 mg/kg/day spironolactone | Starting at 4 or 8 weeks of age, continued until 20 weeks of age | Early treatment significantly improved cardiac and skeletal muscle function, reduced cardiomyocyte damage and fibrosis. | Circulation. 2011 Aug 2;124(5):582-8 |
| Mice | Chronic hypoxia model | Intramuscular injection | 1 μg | 3-5 dpi | To study the effect of ACE inhibitor Lisinopril on muscle regeneration under chronic hypoxia, results showed Lisinopril increased MuSCs proliferation and muscle regeneration | J Cachexia Sarcopenia Muscle. 2024 Apr;15(2):631-645 |
| Mice | Melanoma-induced cachexia model | Oral | 40 mg/L | From the day of cancer cell injection | Lisinopril partially preserved muscle force but did not prevent tissue wasting induced by cachexia. | Cell Rep. 2023 Jan 31;42(1):111934 |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT01936012 | Healthy | Not Applicable | Completed | - | Indonesia ... 展开 >> PT Equilab International Jakarta, Indonesia, 12430 收起 << |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
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1 mM 5 mM 10 mM |
2.26mL 0.45mL 0.23mL |
11.32mL 2.26mL 1.13mL |
22.65mL 4.53mL 2.26mL |
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| CAS号 | 83915-83-7 |
| 分子式 | C21H35N3O7 |
| 分子量 | 441.52 |
| SMILES Code | O=C([C@H]1N(C([C@@H](N[C@H](C(O)=O)CCC2=CC=CC=C2)CCCCN)=O)CCC1)O.O.O |
| MDL No. | MFCD01698825 |
| 别名 | 赖诺普利二水合物 ;MK-521 dihydrate; Lisinopril(dihydrate) |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, 2-8°C |
| 溶解方案 |
H2O: 20 mg/mL(45.3 mM),配合低频超声助溶
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