
Eprosartan Mesylate
CAS No. 144143-96-4
Eprosartan Mesylate( SKF 108566J )
Catalog No. M11872 CAS No. 144143-96-4
Eprosartan is a nonpeptide angiotensin II receptor antagonist.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
10MG | 36 | Get Quote |
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25MG | 57 | Get Quote |
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100MG | 101 | Get Quote |
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200MG | 156 | Get Quote |
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500MG | Get Quote | Get Quote |
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Biological Information
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Product NameEprosartan Mesylate
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NoteResearch use only, not for human use.
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Brief DescriptionEprosartan is a nonpeptide angiotensin II receptor antagonist.
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DescriptionEprosartan is a nonpeptide angiotensin II receptor antagonist, [3H]-eprosartan binds to the AT1 receptor with KD of 0.83 nM in rat vascular smooth muscle cells.(In Vitro):Eprosartan (SKF-108566J) inhibits [125I]AII binding to human liver membranes (IC50 of 1.7 nM) and to rat mesenteric artery membranes (IC50 of 1.5 nM). In rabbit aortic smooth muscle cells, Eprosartan caused a concentration-dependent inhibition of AII-induced increases in intracellular Ca2+ levels.(In Vivo):In conscious normotensive rats, i.v. administration of Eprosartan (0.01-0.3 mg/kg) produced dose-dependent parallel shifts in the AII pressor dose-response curve. Administration of Eprosartan (3-10 mg/kg) intraduodenally or intragastrically to conscious normotensive rats resulted in a dose-dependent inhibition of the pressor response to AII (250 ng/kg, i.v.). At 10 mg/kg, i.d., significant inhibition of the pressor response to AII was observed for 3 hr.
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In VitroEprosartan (SKF-108566J) inhibits [125I]AII binding to human liver membranes (IC50 of 1.7 nM) and to rat mesenteric artery membranes (IC50 of 1.5 nM). In rabbit aortic smooth muscle cells, Eprosartan caused a concentration-dependent inhibition of AII-induced increases in intracellular Ca2+ levels.
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In VivoIn conscious normotensive rats, i.v. administration of Eprosartan (0.01-0.3 mg/kg) produced dose-dependent parallel shifts in the AII pressor dose-response curve. Administration of Eprosartan (3-10 mg/kg) intraduodenally or intragastrically to conscious normotensive rats resulted in a dose-dependent inhibition of the pressor response to AII (250 ng/kg, i.v.). At 10 mg/kg, i.d., significant inhibition of the pressor response to AII was observed for 3 hr.
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SynonymsSKF 108566J
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PathwayEndocrinology/Hormones
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TargetRAAS
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RecptorAT1 receptor
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number144143-96-4
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Formula Weight520.62
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Molecular FormulaC23H24N2O4S·CH4O3S
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Purity>98% (HPLC)
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SolubilityEthanol: 4 mg/mL (7.68 mM); DMSO: 104 mg/mL (199.76 mM)
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SMILESCCCCC1=NC=C(N1CC2=CC=C(C=C2)C(=O)O)/C=C(\CC3=CC=CS3)/C(=O)O.CS(=O)(=O)O
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Chemical Name4-[[2-butyl-5-[(E)-2-carboxy-3-thiophen-2-ylprop-1-enyl]imidazol-1-yl]methyl]benzoic acid;methanesulfonic acid
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.Plosker GL, et al. Drugs, 2000, 60(1), 177-20
molnova catalog



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