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Efonidipine hydrochloride monoethanolate_Molecular_structure_CAS_)
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Efonidipine hydrochloride monoethanolate

Catalog No. E0159 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C36H45ClN3O8P Telephone 1-800-521-8956
M. W. 714.184561 Fax
Purity ≥98% (HPLC) Email
Storage desiccated Chembase ID: 154222

SYNONYMS

IUPAC name
ethanol 2-[benzyl(phenyl)amino]ethyl 5-(5,5-dimethyl-2-oxo-1,3,2λ5-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate hydrochloride
IUPAC Traditional name
efonidipine ethyl alcohol hydrochloride

DATABASE IDS

MDL Number MFCD00875717

PROPERTIES

Empirical Formula (Hill Notation) C34H38N3O7P · HCl · C2H5OH
Purity ≥98% (HPLC)
Apperance pale yellow powder
Solubility DMSO: >5 mg/mL
Solubility H2O: insoluble
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Condition desiccated
Storage Temperature 2-8°C
German water hazard class 1

DETAILS

Description (English)
Biochem/physiol Actions
Racemic efonidipine has both L-type and T-type calcium channel blocking activity. The R(-)-isomer appears to be very selective for T-type calcium channel. The S(+)-isomer inhibits the expressed Ca(V)1.2, Ca(V)1.3 and Ca(V)3.1 channel currents almost equally.1
Description (简体中文)
Biochem/physiol Actions
Racemic efonidipine has both L-type and T-type calcium channel blocking activity. The R(-)-isomer appears to be very selective for T-type calcium channel. The S(+)-isomer inhibits the expressed Ca(V)1.2, Ca(V)1.3 and Ca(V)3.1 channel currents almost equally.1

REFERENCES