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Details

Stereochemistry RACEMIC
Molecular Formula C22H28Cl2N2O6
Molecular Weight 487.374
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OLRADIPINE

SMILES

CCOC(=O)C1=C(COCCOCCN)NC(C)=C(C1C2=CC=CC(Cl)=C2Cl)C(=O)OC

InChI

InChIKey=VLTBMBOHGZAWIT-UHFFFAOYSA-N
InChI=1S/C22H28Cl2N2O6/c1-4-32-22(28)19-16(12-31-11-10-30-9-8-25)26-13(2)17(21(27)29-3)18(19)14-6-5-7-15(23)20(14)24/h5-7,18,26H,4,8-12,25H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C22H28Cl2N2O6
Molecular Weight 487.374
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Olradipine (also known as S 11568) is a L-type Ca(2+) channel antagonist. This drug was being developed in France for the treatment of heart failure, hypertension, and ischemic heart disorder. However, all these studies were discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Ca2+ channel inhibition by a new dihydropyridine derivative, S11568, and its enantiomers S12967 and S12968.
1990 Nov 6
Inhibition of L-type but not T-type calcium channel current by a new dihydropyridine derivative, S11568.
1991 Feb
Ca2+ channel inhibition in a rat osteoblast-like cell line, UMR 106, by a new dihydropyridine derivative, S11568.
1992 Sep 10
Myocardial kinetics of the (11)C-labeled enantiomers of the Ca(2+) channel inhibitor S11568: an in vivo study.
2001 Jun
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:29:36 GMT 2023
Edited
by admin
on Fri Dec 15 16:29:36 GMT 2023
Record UNII
617O238A6V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OLRADIPINE
INN  
INN  
Official Name English
olradipine [INN]
Common Name English
3-ETHYL 5-METHYL (±)-2-((2-(2-AMINOETHOXY)ETHOXY)METHYL)-4-(2,3-DICHLOROPHENYL)-1,4-DIHYDRO-6-METHYL-3,5-PYRIDINEDICARBOXYLATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
Code System Code Type Description
CAS
115972-78-6
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID40921881
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
PUBCHEM
131532
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
FDA UNII
617O238A6V
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
INN
7081
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104881
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
SMS_ID
100000083316
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
EVMPD
SUB09435MIG
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
NCI_THESAURUS
C84033
Created by admin on Fri Dec 15 16:29:36 GMT 2023 , Edited by admin on Fri Dec 15 16:29:36 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY