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
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
Approval Year
PubMed
Title | Date | PubMed |
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Ca2+ channel inhibition by a new dihydropyridine derivative, S11568, and its enantiomers S12967 and S12968. | 1990 Nov 6 |
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Inhibition of L-type but not T-type calcium channel current by a new dihydropyridine derivative, S11568. | 1991 Feb |
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Ca2+ channel inhibition in a rat osteoblast-like cell line, UMR 106, by a new dihydropyridine derivative, S11568. | 1992 Sep 10 |
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Myocardial kinetics of the (11)C-labeled enantiomers of the Ca(2+) channel inhibitor S11568: an in vivo study. | 2001 Jun |
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NCI_THESAURUS |
C333
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SUB09435MIG
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C84033
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ACTIVE MOIETY