Efonidipine hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: I000444
  • CAS Number: 111011-53-1
  • Molecular Formula: C34H39ClN3O7P
  • Molecular Weight: 668.12
  • Purity: ≥95%
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Efonidipine hydrochloride (Cat.No:I000444) is a calcium channel blocker used in the treatment of hypertension and angina pectoris. It acts by blocking calcium channels in smooth muscle cells, resulting in vasodilation and lowering of blood pressure. Efonidipine hydrochloride also exhibits additional vasoprotective effects, making it a valuable option for managing cardiovascular conditions.


Catalog Number I000444
CAS Number 111011-53-1
Molecular Formula C34H39ClN3O7P
Purity ≥95%
Target Neuronal Signaling
Solubility DMSO: ≤ 8.5 mg/mL
Storage Store at -20°C
IUPAC Name 2-(N-benzylanilino)ethyl 5-(5,5-dimethyl-2-oxo-1,3,2lambda5-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate;hydrochloride
InChI InChI=1S/C34H38N3O7P.ClH/c1-24-30(33(38)42-19-18-36(28-15-9-6-10-16-28)21-26-12-7-5-8-13-26)31(27-14-11-17-29(20-27)37(39)40)32(25(2)35-24)45(41)43-22-34(3,4)23-44-45;/h5-17,20,31,35H,18-19,21-23H2,1-4H3;1H
InChIKey OXVTXPCIJDYQIS-UHFFFAOYSA-N
SMILES CC1=C(C(C(=C(N1)C)P2(=O)OCC(CO2)(C)C)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OCCN(CC4=CC=CC=C4)C5=CC=CC=C5.Cl
Reference

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<br>[1]. Ikeda K, et al. Efonidipine, a Ca(2+)-channel blocker, enhances the production of dehydroepiandrosterone sulfate in NCI-H295R human adrenocortical carcinoma cells. Tohoku J Exp Med. 2011;224(4):263-71.
<br>[2]. Nakano N, et al. Effects of efonidipine, an L- and T-type calcium channel blocker, on the renin-angiotensin-aldosterone system in chronic hemodialysis patients. Int Heart J. 2010 May;51(3):188-92.
<br>[3]. Suzuki S, et al. Beneficial effects of the dual L- and T-type Ca2+ channel blocker efonidipine on cardiomyopathic hamsters. Circ J. 2007 Dec;71(12):1970-6.
<br>[4]. Lee TS, et al. Actions of mibefradil, efonidipine and nifedipine block of recombinant T- and L-type Ca channels with distinct inhibitory mechanisms. Pharmacology. 2006;78(1):11-20.
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