Details
Stereochemistry | RACEMIC |
Molecular Formula | C26H36N2O3 |
Molecular Weight | 424.5756 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC(CCN(C)CCCC(C#N)(C(C)C)C2=CC(OC)=C(OC)C=C2)=C1
InChI
InChIKey=VMVKIDPOEOLUFS-UHFFFAOYSA-N
InChI=1S/C26H36N2O3/c1-20(2)26(19-27,22-11-12-24(30-5)25(18-22)31-6)14-8-15-28(3)16-13-21-9-7-10-23(17-21)29-4/h7,9-12,17-18,20H,8,13-16H2,1-6H3
Approval Year
PubMed
Title | Date | PubMed |
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Opposite effects of a single IIIS5 mutation on phenylalkylamine and dihydropyridine interaction with L-type Ca2+ channels. | 2004 Dec 31 |
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L-type Ca2+ channel antagonists block voltage-dependent Ca2+ channels in identified leech neurons. | 2004 Jul 9 |
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Pharmacophoric features and Ca2+ ion holding capacity of verapamil. | 2005 Dec 15 |
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Investigation of the phenylalkylamine binding site in hKv1.3 (H399T), a mutant with a reduced C-type inactivated state. | 2005 Oct |
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Structural model for phenylalkylamine binding to L-type calcium channels. | 2009 Oct 9 |
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NCI_THESAURUS |
C333
Created by
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SUB07015MIG
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CHEMBL2074792
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C77823
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Devapamil
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92302-55-1
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102268-75-7
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SUPERSEDED |
ACTIVE MOIETY