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efonidipine

Known as: 3-Pyridinecarboxylic acid, 5-(5,5-dimethyl-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 2-(phenyl(phenylmethyl)amino)ethyl ester, P-oxide, monohydrochloride, 5-(5,5-dimethyl-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-pyridinecarboxylic acid, 2-(phenyl(phenylmethyl)amino) ethyl ester, P-oxide, hydrochloride 
National Institutes of Health

Papers overview

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Review
2007
Review
2007
A large body of evidence has accrued indicating that voltage-gated Ca(2+) channel subtypes, including L-, T-, N-, and P/Q-type… 
2006
2006
We compared detailed efficacy of efonidipine and nifedipine, dihydropyridine analogues, and mibefradil using recombinant T- and L… 
2006
2006
Targeting aldosterone synthesis and/or release represents a potentially useful approach to the prevention of cardiovascular… 
Highly Cited
2004
Highly Cited
2004
Efonidipine, a derivative of dihydropyridine Ca2+ antagonist, is known to block both L‐ and T‐type Ca2+ channels. It remains to… 
Highly Cited
2003
Highly Cited
2003
Aldosterone (Aldo) accelerates hypertension, proteinuria, and glomerulosclerosis in animal models of malignant hypertension or… 
Highly Cited
2002
Highly Cited
2002
We compared the levels of microparticles, platelet activation markers, soluble cell adhesion molecules, and soluble selectins… 
2000
2000
The influence of hypertension and of treatment with some dihydropyridine-type Ca(2+) channel blockers and with the…