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eprosartan

Known as: Éprosartan, (e)-2-Butyl-1-(P-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid, 2-Thiophenepropanoic acid, alpha-((2-butyl-1-((4- carboxyphenyl)methyl)-lH-imidazol-5-yl)methylene)-, (E)- 
A competitive and reversible angiotensin II receptor antagonist with anti-hypertensive property. Eprosartan blocks the binding of angiotensin II to… Expand
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
BACKGROUND Recent data suggest that atenolol may be inferior to other antihypertensive drugs in reducing cardiovascular risk in… Expand
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Highly Cited
2006
Highly Cited
2006
Tissue accumulation of circulating prorenin results in angiotensin generation, but could also, through binding to the recently… Expand
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Highly Cited
2005
Highly Cited
2005
Background and Purpose— In hypertensive stroke patients, for the same level of blood pressure control, eprosartan will be more… Expand
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Highly Cited
2005
Highly Cited
2005
Angiotensin-converting enzyme (ACE)-2 is a newly described enzyme with antagonistic effects to those of the classical ACE (ACE-1… Expand
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Highly Cited
2005
Highly Cited
2005
The adipose-specific protein adiponectin has been recently discovered to improve insulin sensitivity. Angiotensin type-1 receptor… Expand
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Highly Cited
2004
Highly Cited
2004
Background—Angiotensin type 1 receptor (AT1R) blockers (ARB) have been shown to reduce the incidence of type 2 diabetes mellitus… Expand
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Highly Cited
2004
Highly Cited
2004
We evaluated the antihypertensive activity, glucose homeostasis and plasma lipid profile in patients with mild hypertension and… Expand
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Highly Cited
2004
Highly Cited
2004
Enalapril and losartan reduce but not normalize sympathetic hyperactivity in patients with hypertensive chronic renal failure… Expand
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Highly Cited
1997
Highly Cited
1997
It is well established that angiotensin II can enhance sympathetic nervous system function by activating prejunctional… Expand
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Highly Cited
1997
Highly Cited
1997
To investigate the effect of steady‐state fluconazole administration on the disposition of eprosartan, losartan, and E‐3174. 
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