Metroprolol Succinate
Cat.No:IM2900 Solarbio
CAS:98418-47-4
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:≥98%
Appearance:Solid
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Metroprolol SuccinateCAS:98418-47-4
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:≥98%
Appearance:Solid
Qty:
Size:
CAS | 98418-47-4 |
Name | Metroprolol Succinate |
Molecular Formula | C34H56N2O10 |
Molecular Weight | 652.82 |
Solubility | Soluble in Water/DMSO(Need ultrasonic) |
Purity | ≥98% |
Appearance | Solid |
Storage | Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
MDL | MFCD07391179 |
SMILES | CC(C)NCC(COC1=CC=C(C=C1)CCOC)O.CC(C)NCC(COC1=CC=C(C=C1)CCOC)O.C(CC(=O)O)C(=O)O |
InChIKey | RGHAZVBIOOEVQX-UHFFFAOYSA-N |
InChI | InChI=1S/2C15H25NO3.C4H6O4/c2*1-12(2)16-10-14(17)11-19-15-6-4-13(5-7-15)8-9-18-3;5-3(6)1-2-4(7)8/h2*4-7,12,14,16-17H,8-11H2,1-3H3;1-2H2,(H,5,6)(H,7,8) |
PubChem CID | 62937 |
Target Point | Adrenergic Receptor |
Passage | Endocrinology & Hormones;GPCR & G Protein;Neuronal Signaling |
Background | It is a selective β1-adrenoceptor antagonist. |
Biological Activity | Metroprolol Succinate 是一种口服活性、选择性β1-肾上腺素受体拮抗剂,具有抗炎、抗肿瘤和抗血管生成的特性。[1-3] |
In Vitro | 美托洛尔对 U937 和 MOLT-4 细胞的细胞毒性作用具有剂量和时间依赖性。在 1000μg/ml(3740.14μM)浓度下,美托洛尔能明显降低 U937 和 MOLT-4 细胞在培养 48 小时后的存活率(P<0.01)。此外,当美托洛尔浓度≥500 μg/ml(≥1870.07μM)时,孵育 72 小时后,美托洛尔能明显降低 U937 细胞的活力(P<0.001)。此外,在≥100 μg/ml(≥374.01μM)浓度下,美托洛尔在孵育 72 小时后会明显降低 MOLT-4 细胞的活力(P<0.001)。[3] |
In Vivo | 雄性载脂蛋白E(-/-)小鼠通过渗透压微型泵接受美托洛尔(2.5 毫克/千克/小时)或生理盐水治疗 11 周。能显著减少载脂蛋白E(-/-)小鼠胸主动脉动脉粥样硬化斑块的面积,还能降低血清中促炎细胞因子 TNFα 和 CXCL1 的水平以及斑块中巨噬细胞的含量。[1]美托洛尔(15 mg/kg/q12h;静脉注射;5 天)在柯萨奇病毒 B3 诱导的病毒性心肌炎小鼠模型中显示出抗炎和抗病毒作用。[2]美托洛尔和 ZLF 可通过抑制细胞凋亡/线粒体凋亡途径,在 冠状动脉微栓塞(CME)期间通过抑制细胞凋亡和改善心功能来保护大鼠心肌。[4] |
Cell Experiment | 将人类白血病 T 细胞(MOLT-4)和单核细胞(U937)培养在(RPMI)1640 完全培养基中。然后用不同浓度的美托洛尔(1、10、50、100、500 和 1000 μg/ml)处理培养的 U937 和 MOLT-4 细胞 24、48 和 72 小时。采用 MTT(3-[4,5 dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide)法测定美托洛尔的细胞毒性。[3] |
Animal Experiment | 96只小鼠腹腔接种CVB3诱导VMC。接种 CVB3 的小鼠平均分为心肌炎组(32 只)、卡维地洛组(32 只)和美托洛尔组(32 只)。20 只小鼠(对照组)腹腔注射生理盐水。采用血红素和伊红染色及组织病理学评分法研究卡维地洛和美托洛尔对第 3 天和第 5 天心肌组织病理学变化的影响。此外,在第 3 天和第 5 天,分别使用化学发光免疫分析法、酶联免疫吸附分析法和斑块分析法测定血清 cTn-I 水平、细胞因子水平和病毒滴度。最后,在第 5 天使用免疫组化染色法和 Western 印迹法研究磷酸化 p38MAPK 的水平。[2] |
Data Literature Source | [1]. Ulleryd MA,et al. Metoprolol reduces proinflammatory cytokines and atherosclerosis in ApoE-/- mice. Biomed Res Int. 2014;2014:548783. [2]. Wang D,et al. Carvedilol has stronger anti-inflammation and anti-virus effects than metoprolol in murine model with coxsackievirus B3-induced viral myocarditis. Gene. 2014 Sep 1;547(2):195-201. [3]. Hajatbeigi B,et al. Cytotoxicity of metoprolol on leukemic cells in vitro[J]. 2018. [4]. Su Q,et al. Effect of metoprolol on myocardial apoptosis and caspase-9 activation after coronary microembolization in rats. Exp Clin Cardiol. 2013 Spring;18(2):161-5. |
Unit | Bottle |
Specification | 10mg 50mg |
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
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3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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