Metoprolol
CAS No. 51384-51-1
Metoprolol( Metoprolol | Loresor | Preblok | Metohexal | Selo-Zok )
Catalog No. M14778 CAS No. 51384-51-1
A selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameMetoprolol
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NoteResearch use only, not for human use.
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Brief DescriptionA selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension.
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DescriptionA selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension.Hypertension Approved.
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In VitroMetoprolol (0-1000 μg/mL; 24-72 h) shows cytotoxic effect on U937 and MOLT-4 cells dose and time dependently.Cell Cytotoxicity Assay Cell Line:U937 and MOLT-4 cellsConcentration:1, 10, 50, 100, 500 and 1000 μg/mL Incubation Time:24, 48 and 72 h Result:Significantly decreased the viability of U937 and MOLT-4 cells at 1000 μg/mL (3740.14μM) concentration after 48 hours incubation time, significantly reduced the viability of U937 cells at ≥500 μg/ml (≥1870.07μM) concentrations after 72 hours incubation time, and significantly decreased the viability of MOLT4 cells at ≥100 μg/ml (≥374.01μM) concentrations after 72 hours incubation.
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In VivoMetoprolol (2.5 mg/kg/h; infusion; 11 weeks) reduces proinflammatory cytokines and atherosclerosis in ApoE?/? Mice.Metoprolol (15 mg/kg/q12h; i.g.; 5 days) shows anti-inflammation and anti-virus effects in murine model with coxsackievirus B3-induced viral myocarditis.Metoprolol (2.5 mg/kg; i.v.; 3 bolus injections) significantly decreased activated caspase-9 protein expression and inhibits myocardial apoptosis in coronary microembolization (CME) rats. Animal Model:Male ApoE?/? mice Dosage:2.5?mg/kg/h Administration:Via osmotic minipumps, 11 weeks Result:Significantly reduced atherosclerotic plaque area in thoracic aorta, reduced serum TNFα and the chemokine CXCL1 as well as decreasing the macrophage content in the plaques.Animal Model:Balb/c mice, coxsackievirus B3 (CVB3) induced viral myocarditis (VMC) model Dosage:15 mg/kg/q12h Administration:Oral gavage, 5 consecutive days Result:Reduced pathological scores of VMC induced by CVB3 infection, protected the myocardium against viral damage by reducing serum cTn-I levels. Decreased the levels of myocardial pro-inflammatory cytokines and increase the expression of anti-inflammatory cytokine. Significantly decreased myocardial virus titers.
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SynonymsMetoprolol | Loresor | Preblok | Metohexal | Selo-Zok
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PathwayGPCR/G Protein
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TargetAdrenergic Receptor
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RecptorAdrenergic Receptor
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Research AreaCardiovascular Disease
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IndicationHypertension
Chemical Information
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CAS Number51384-51-1
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Formula Weight267.3639
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Molecular FormulaC15H25NO3
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Purity>98% (HPLC)
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SolubilityDMSO
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SMILESOC(COC1=CC=C(CCOC)C=C1)CNC(C)C
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Chemical Name2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
molnova catalog
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