Manidipine dihydrochloride

Manidipine dihydrochloride (Manidipine 2HCl) 是一种钙离子通道阻断剂,能抑制钙流,IC50=2.6 nM。

CAS号

89226-75-5

分子式

C35H40Cl2N4O6

主要靶点

Calcium Channel

仅限科研使用

Cat No : CM03238

Print datasheet

Synonyms

盐酸马尼地平|CV-4093|Manidipine 2HCl



产品信息

Manidipine dihydrochloride is a potent calcium channel blocker for Ca2+ current(IC50=2.6 nM).

CAS号 89226-75-5
分子式 C35H40Cl2N4O6
主要靶点 Calcium Channel
主要通路 代谢|离子通道
分子量 683.62
纯度 100.00%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 盐酸马尼地平|CV-4093|Manidipine 2HCl

靶点活性

Calcium channel:2.6 nM

体内活性

在高血压大鼠中,口服 Manidipine(3 mg/kg和10 mg/kg)以剂量依赖性的方式降低大鼠的收缩压.Manidipine(10 mg/kg)给药1小时到3小时后,能够将血压降低到正常水平.

体外活性

在纳摩尔级浓度的Manidipine,能够有效调节参与系膜细胞促炎性变化的基因转录。Manidipine抑制冠状动脉(pIC50=9.3 nM)和肾动脉(pIC50=9.1 nM)。Manidipine在高于0.1 nM浓度时降低Ca2+流,在100 nM浓度时阻断Ca2+流。

溶解度

Ethanol:<1 mg/mL,H2O:<1 mg/mL,DMSO:20 mg/mL (29.3 mM)

细胞实验

The mitogenic effect is measured by the amout of [3H]thymidine incorporated into DNA of human MCs and by assessment of cell proliferation. In brief, 1 × 105 quiescent cells is seeded into a 25-mL cell culture bottle and kept in low serum medium (0.1% FCS). On the following day, the cells are preincubated for 3 hours with Manidipine (10 nM) followed by stimulation with PDGF-BB (10 ng/mL) or incubated with low serum medium abone. The medium is replaced each day, and the cells are counted at days 1, 3 and 5.(Only for Reference)

参考文献

1.Tohse N, et al. Eur J Pharmacol, 1993, 249(2), 231-233.
2.Pfaffendorf M, et al. Am Heart J, 1993, 125(2 Pt 2), 571-577.
3.Iimura O, et al. Am Heart J, 1993, 125(2 Pt 2), 635-641.
4.Roth M, et al. Proc Natl Acad Sci, 1992, 89(9), 4071-4075.
5.Kakihana M, et al. Jpn J Pharmacol, 1988, 48(2), 223-228.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
×
=
×
C1   V1   C2   V2