
Trandolapril
CAS No. 87679-37-6
Trandolapril ( RU44570 )
产品货号. M28471 CAS No. 87679-37-6
群多普利是一种口服血管紧张素转换酶 (ACE) 抑制剂,可水解为活性二酸群多普利拉。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥316 | 有现货 |
![]() ![]() |
10MG | ¥518 | 有现货 |
![]() ![]() |
25MG | ¥932 | 有现货 |
![]() ![]() |
50MG | ¥1596 | 有现货 |
![]() ![]() |
100MG | ¥2535 | 有现货 |
![]() ![]() |
200MG | ¥3791 | 有现货 |
![]() ![]() |
500MG | ¥6099 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Trandolapril
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述群多普利是一种口服血管紧张素转换酶 (ACE) 抑制剂,可水解为活性二酸群多普利拉。
-
产品描述Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that is hydrolysed to the active diacid trandolaprilat.
-
体外实验Trandolapril (0.02 mM, 1 mM; 3 d) inhibits cell growth and induces cell apoptosis, increases the percentage of apoptotic cells in K562 cell line. Apoptosis Analysis Cell Line:K562, KU812, U937 and HL60 Concentration:0-2 mM Incubation Time:0, 1, 2, 3 days Result:Inhibited K562, KU812, U937 at 1 mM and inhibited HL60 at 0.02 mM.
-
体内实验Trandolapril (3 mg/kg/day; p.o.; 7 d) reduces renal fibrosis in obstructive nephropathy in mice, by inhibiting renal interstitial matrix expression and myofibroblast activation, decreasing renal proinflammatory cytokine RANTES and TNF-α level.Trandolapril (0.3 mg/kg/day; p.o.; 4 weeks) improves arterial mechanics in rats, prevents arterial hypertrophy, collagen and cellular fibronectin accumulation.randolapril (0.3 mg/kg/day; p.o.; 4 months) exhibits a chronic anti-hypertension effects in rats, results in blood pressure decreasing.Trandolapril (0.25 mg/kg; p.o.; twice a day; 4 months) inhibits Atherosclerosis in the Watanabe Heritable Hyperlipidemic Rabbit. Animal Model:UUD (unilateral ureteral obstruction) model in Male CD-1 mice (18-22 g) Dosage:3 mg/kg Administration:Oral gavage; daily, for 7 days Result:Resulted in renal interstitial matrix expression (including fibronectin, type I, and type III collagen) decreasing, and inhibited myofibroblast activation by surprising a-smooth muscle actin (a-SMA) expression, decreased the RANTES (regulated on activation, normal T cell expressed and secreted) and TNF-α level.Animal Model:SHR model (spontaneously hypertensive rats, 4-week-old) Dosage:0.3 mg/kg Administration:Oral gavage; daily for 4 weeks Result:Reduced collagen content in the aortic media and increased ariterial distensibility up to about 80%.Animal Model:Watanabe heritable hyperlipidemic rabbit (3 months old)Dosage:0.25 mg/kg Administration:Oral gavage; twice a day; 9 months Result:Decreased in atherosclerotic involvement of the intimal surface, and also decreased cholesterol content in descending thoracic aorta.
-
同义词RU44570
-
通路Metabolic Enzyme/Protease
-
靶点ACE
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number87679-37-6
-
分子量430.545
-
分子式C24H34N2O5
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (232.27 mM)
-
SMILESCCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1[C@H]2CCCC[C@@H]2C[C@H]1C(O)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册




关联产品
-
Lisinopril dihydrate
一种血管紧张素转换酶 (ACE) 抑制剂,用于治疗高血压、心力衰竭和心脏病发作后的症状。
-
Omapatrilat
金属蛋白酶 ACE 和 NEP 的有效双重抑制剂,Ki 分别为 0.64 nM 和 0.45 nM。
-
Temocaprilat
Temocaprilat 是一种血管紧张素转换酶 (ACE) 抑制剂。