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Details

Stereochemistry RACEMIC
Molecular Formula C29H33FN2O6.ClH
Molecular Weight 561.041
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELGODIPINE HYDROCHLORIDE

SMILES

Cl.CC(C)OC(=O)C1=C(C)NC(C)=C(C1C2=CC=CC3=C2OCO3)C(=O)OCCN(C)CC4=CC=C(F)C=C4

InChI

InChIKey=JBKDMKOYLBVOOR-UHFFFAOYSA-N
InChI=1S/C29H33FN2O6.ClH/c1-17(2)38-29(34)25-19(4)31-18(3)24(26(25)22-7-6-8-23-27(22)37-16-36-23)28(33)35-14-13-32(5)15-20-9-11-21(30)12-10-20;/h6-12,17,26,31H,13-16H2,1-5H3;1H

HIDE SMILES / InChI
Elgodipine (IQB-875, CAS 119413-55-7) is a phenyldihydropyridine derivative acting as a calcium channel antagonist. Elgodipine inhibited both T- and L-type calcium channels in a concentration-dependent manner. Elgodipine was in clinical trials for the treatment of cardiovascular diseases however its development has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cardiovascular effects of elgodipine and nifedipine compared in anaesthetized rats.
1997-09-24
Electrophysiological and radioligand binding studies of elgodipine and derivatives in portal vein myocytes.
1994-12
Cardiovascular effects of the new dihydropyridine derivative elgodipine.
1991-09
Patents

Sample Use Guides

Pharmacokinetic study: elgodipine was given as continuous infusion at various rates (5, 10, 15, 20, 40 microg/kg/h for 48, 48, 48, 24, or 6 h, respectively) to five groups of 6-12 healthy male subjects (total 42).
Route of Administration: Intravenous
In Vitro Use Guide
Elgodipine inhibited both T- and L-type calcium channels in a concentration-dependent manner. Half-inhibitions of T- and L-type calcium channel current were obtained at concentrations of 32 and 2.3 nM, respectively.
Name Type Language
IQB-875
Preferred Name English
ELGODIPINE HYDROCHLORIDE
MI  
Common Name English
2-((P-FLUOROBENZYL)METHYLAMINO)ETHYL ISOPROPYL (±)- 1,4-DIHYDRO-2,6-DIMETHYL-4-(2,3-(METHYLENEDIOXY)PHENYL)-3,5-PYRIDINEDICARBOXYLATE HYDROCHLORIDE
Common Name English
ELGODIPINE HYDROCHLORIDE [MI]
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 4-(1,3-BENZODIOXOL-4-YL)-1,4-DIHYDRO-2,6-DIMETHYL-, 3-(2-(((4-FLUOROPHENYL)METHYL)METHYLAMINO)ETHYL) 5-(1-METHYLETHYL) ESTER, HYDROCHLORIDE (1:1)
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 4-(1,3-BENZODIOXOL-4-YL)-1,4-DIHYDRO-2,6-DIMETHYL-, 2-(((4-FLUOROPHENYL)METHYL)METHYLAMINO)ETHYL 1-METHYLETHYL ESTER, MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
CAS
121489-04-1
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
PRIMARY
MESH
C063839
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
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PUBCHEM
3078492
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
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MERCK INDEX
m1130
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
PRIMARY Merck Index
FDA UNII
MIR106H7SI
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
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EPA CompTox
DTXSID60923822
Created by admin on Mon Mar 31 18:13:48 GMT 2025 , Edited by admin on Mon Mar 31 18:13:48 GMT 2025
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