Manidipine dihydrochloride
CAS No. 89226-75-5
Manidipine dihydrochloride ( CV-4093 )
产品货号. M16434 CAS No. 89226-75-5
一种二氢吡啶型钙通道阻滞剂,用作抗高血压药。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥253 | 有现货 |
|
| 50MG | ¥349 | 有现货 |
|
| 100MG | ¥577 | 有现货 |
|
| 500MG | ¥1436 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥392 | 有现货 |
|
生物学信息
-
产品名称Manidipine dihydrochloride
-
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
-
产品简述一种二氢吡啶型钙通道阻滞剂,用作抗高血压药。
-
产品描述A dihydropyridine type calcium channel blocker that is used as an antihypertensive.Hypertension Approved.
-
体外实验——
-
体内实验Animal Model:IFNAR-/- miceDosage:10 mg/kg Administration:Intraperitoneal injection (i.p. ), b.i.d. at day 4, day 5 Result:Exhibited a modest, but statistically significant increase in the survival rate of lethal animal model with SFTSV infection, significantly reduced viral titers in the spleen and kidney.Animal Model:Adult female BALB/c mice (age, 4 weeks) Dosage:25 mg/kg Administration:Intraperitoneal injection (i.p. ), b.i.d. for 2 days, then daily for 19 days Result:Reduced the mortality rate from 73% to 20%, significantly reduced the viral load in infected mice while remarkably alleviated brain damage phenomena. Had little effect on peripheral JEV infection, which indicated that manidipine protected the mice against JEV-induced lethality by decreasing the viral load in the brain.Animal Model:8-week-old male Wistar rats Dosage:3 mg/kg Administration:Intragastric gavage (i.g.), once per day for 7 d Result:Prevented isoproterenol-induced left ventricular hypertrophy (2.26±0.02 g/kg;p<0.01) as isoproterenol increased left ventricular weight (2.40±0.04 g/kg; p<0.01). Inhibited expression of mRNA of ANP (0.9-fold of the control value; p<0.01), collagen types I (1.1-fold; p<0.01) and type III (1.6-fold; p<0.01), and fibronectin (1.1-fold; p<0.01).
-
同义词CV-4093
-
通路GPCR/G Protein
-
靶点Calcium Channel
-
受体CalciumChannel
-
研究领域Cardiovascular Disease
-
适应症Hypertension
化学信息
-
CAS Number89226-75-5
-
分子量683.6213
-
分子式C35H40Cl2N4O6
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILES[H+].[H+].[Cl-].[Cl-].COC(=O)C1=C(C)NC(C)=C(C1C1=CC(=CC=C1)[N+]([O-])=O)C(=O)OCCN1CCN(CC1)C(C1=CC=CC=C1)C1=CC=CC=C1
-
化学全称3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 3-[2-[4-(diphenylmethyl)-1-piperazinyl]ethyl] 5-methyl ester, hydrochloride (1:2)
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
1. Cheer SM, et al. Drugs. 2001;61(12):1777-99.
2. Roca-Cusachs A, et al. Drugs. 2005;65 Suppl 2:11-9.
产品手册
关联产品
-
Dimethadione
一种抗惊厥药,是曲美沙丁的活性代谢产物。
-
Mirogabalin besylate
Mirogabalin besylate (DS-5565) 是电压门控钙通道 α2δ 亚基的一种新型有效选择性配体,对于人类 α2δ-1、人类 α2δ-2、大鼠 α2δ-1 的 Kd 为 13.5/22.7/27.0/47.6 nM和大鼠α2δ-2亚基,分别。
-
Imagabalin
Imagabalin (PD 0332334) 是电压依赖性钙通道 (VDCC) α2δ 亚基的新型配体,对 α2δ1 亚基比 α2δ2 具有一定选择性。
021-51111890
购物车()
sales@molnova.cn

