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144628-52-4

144628-52-4 Structure

144628-52-4 Structure
IdentificationBack Directory
[Name]

1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)carbonyl]amino]sulfonyl][1,1'-biphenyl]-4-yl]methyl]-
[CAS]

144628-52-4
[Synonyms]

HR720
HR-720
HOE720
HOE-720
Fonsartan free acid
1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)carbonyl]amino]sulfonyl][1,1'-biphenyl]-4-yl]methyl]-
[Molecular Formula]

C26H32N4O5S2
[MOL File]

144628-52-4.mol
[Molecular Weight]

544.69
Chemical PropertiesBack Directory
[density ]

1.31±0.1 g/cm3(Predicted)
[pka]

1.93±0.36(Predicted)
Hazard InformationBack Directory
[Uses]

Fonsartan (HOE-720) free acid is an orally active angiotensin II receptor (AT1R) antagonist with an IC50 value of 0.48 nM, exhibiting potent antihypertensive activity. Fonsartan free acid dose-dependently inhibits angiotensin II-induced pressor response in rats (ID50 = 0.11 mg/kg) and shows significant long-lasting blood pressure-lowering effects in high-renin animal models. Fonsartan free acid is primarily used in research on hypertension and cardiovascular diseases[1].
[References]

[1] Deprez P, et al. Sulfonylureas and sulfonylcarbamates as new non-tetrazole angiotensin II receptor antagonists. Discovery of a highly potent orally active (imidazolylbiphenylyl)sulfonylurea (HR 720). J Med Chem. 1995 Jun 23;38(13):2357-77. DOI:10.1021/jm00013a013
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