
Bepridil hydrochloride
CAS No. 68099-86-5
Bepridil hydrochloride( CERM 1978 )
Catalog No. M20140 CAS No. 68099-86-5
Bepridil is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX) sodium channels and cardiac sarcolemmal KATP channels.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 37 | In Stock |
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10MG | 49 | In Stock |
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25MG | 88 | In Stock |
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50MG | 122 | In Stock |
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100MG | 170 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameBepridil hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionBepridil is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX) sodium channels and cardiac sarcolemmal KATP channels.
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DescriptionBepridil is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX) sodium channels and cardiac sarcolemmal KATP channels.(In Vitro):Bepridil hydrochloride is a calcium channel blocker, with antianginal activity.(In Vivo):Bepridil hydrochloride (21 mg/kg) reduces heart rate and mean arterial pressure, decreases the mean coronary vascular resistance and increases stroke volume in rats.
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In VitroBepridil hydrochloride is a calcium channel blocker, with antianginal activity.
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In VivoBepridil hydrochloride (21 mg/kg) reduces heart rate and mean arterial pressure, decreases the mean coronary vascular resistance and increases stroke volume in rats.
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SynonymsCERM 1978
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research AreaCardiovascular Disease
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IndicationAngina pectoris; Tachycardia
Chemical Information
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CAS Number68099-86-5
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Formula Weight403
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Molecular FormulaC24H35ClN2O
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Purity>98% (HPLC)
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SolubilityDMSO: 130 mg/mL (322.58 mM)
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SMILESCl.CC(C)COCC(CN(Cc1ccccc1)c1ccccc1)N1CCCC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Flaim SF et al. Effects of bepridil hydrochloride on cardiocirculatory dynamics coronary vascular resistance and cardiac output distribution in normal conscious rats. J Cardiovasc Pharmacol. 1988 Mar;11(3):363-72.
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