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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
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Related topics
Related topics
10 relations
Broader (7)
Antihypertensive Agents
Calcium Channel Blockers
Dihydropyridines
Diuretics
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Efonidipine Hydrochloride
Narrower (2)
NZ 105
enfonidipine hydrochloride
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Five different profiles of dihydropyridines in blocking T-type Ca(2+) channel subtypes (Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I))) expressed in Xenopus oocytes.
T. Furukawa
,
T. Nukada
,
+5 authors
T. Isshiki
European Journal of Pharmacology
2009
Corpus ID: 34169745
2008
2008
T-type Ca2+ channel blockers prevent cardiac cell hypertrophy through an inhibition of calcineurin-NFAT3 activation as well as L-type Ca2+ channel blockers.
M. Horiba
,
Takao Muto
,
+7 authors
K. Yasui
Life Science
2008
Corpus ID: 32833193
Review
2007
Review
2007
Ca2+ channel subtypes and pharmacology in the kidney.
K. Hayashi
,
S. Wakino
,
N. Sugano
,
Y. Ozawa
,
K. Homma
,
T. Saruta
Circulation Research
2007
Corpus ID: 6657651
A large body of evidence has accrued indicating that voltage-gated Ca(2+) channel subtypes, including L-, T-, N-, and P/Q-type…
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2006
2006
Actions of Mibefradil, Efonidipine and Nifedipine Block of Recombinant T- and L-Type Ca2+ Channels with Distinct Inhibitory Mechanisms
Tae-Seong Lee
,
T. Kaku
,
+5 authors
K. Ono
Pharmacology
2006
Corpus ID: 32072510
We compared detailed efficacy of efonidipine and nifedipine, dihydropyridine analogues, and mibefradil using recombinant T- and L…
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2006
2006
Inhibitory Effect of Efonidipine on Aldosterone Synthesis and Secretion in Human Adrenocarcinoma (H295R) Cells
K. Imagawa
,
Satoshi Okayama
,
+6 authors
Yoshihiko Saito
Journal of Cardiovascular Pharmacology
2006
Corpus ID: 46199158
Targeting aldosterone synthesis and/or release represents a potentially useful approach to the prevention of cardiovascular…
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Highly Cited
2004
Highly Cited
2004
Identification of R(−)‐isomer of efonidipine as a selective blocker of T‐type Ca2+ channels
T. Furukawa
,
R. Miura
,
+5 authors
T. Nukada
British Journal of Pharmacology
2004
Corpus ID: 20187659
Efonidipine, a derivative of dihydropyridine Ca2+ antagonist, is known to block both L‐ and T‐type Ca2+ channels. It remains to…
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Highly Cited
2003
Highly Cited
2003
Nongenomic vascular action of aldosterone in the glomerular microcirculation.
S. Arima
,
K. Kohagura
,
+5 authors
S. Ito
Journal of the American Society of Nephrology
2003
Corpus ID: 29308967
Aldosterone (Aldo) accelerates hypertension, proteinuria, and glomerulosclerosis in animal models of malignant hypertension or…
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Highly Cited
2002
Highly Cited
2002
Effects of efonidipine on platelet and monocyte activation markers in hypertensive patients with and without type 2 diabetes mellitus
Shosaku Nomura
,
S. Kanazawa
,
Shiro Fukuhara
Journal of Human Hypertension
2002
Corpus ID: 19864330
We compared the levels of microparticles, platelet activation markers, soluble cell adhesion molecules, and soluble selectins…
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Highly Cited
2002
Highly Cited
2002
Effects of 12 Ca2+ antagonists on multidrug resistance, MDR1-mediated transport and MDR1 mRNA expression.
K. Takara
,
T. Sakaeda
,
+7 authors
K. Okumura
European Journal of Pharmaceutical Sciences
2002
Corpus ID: 22371194
2000
2000
Nephroprotective effect of treatment with calcium channel blockers in spontaneously hypertensive rats.
M. Sabbatini
,
L. Vitaioli
,
Emilia Baldoni
,
Francesco Amenta
Journal of Pharmacology and Experimental…
2000
Corpus ID: 6751310
The influence of hypertension and of treatment with some dihydropyridine-type Ca(2+) channel blockers and with the…
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