Details
Stereochemistry | RACEMIC |
Molecular Formula | C25H35NO4 |
Molecular Weight | 413.5497 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(C)(C)NCC(O)COC1=C(OC)C=CC(CCC(=O)C2=CC=C(C)C=C2)=C1
InChI
InChIKey=WUUQBRHWNUFEEB-UHFFFAOYSA-N
InChI=1S/C25H35NO4/c1-6-25(3,4)26-16-21(27)17-30-24-15-19(10-14-23(24)29-5)9-13-22(28)20-11-7-18(2)8-12-20/h7-8,10-12,14-15,21,26-27H,6,9,13,16-17H2,1-5H3
Alprafenone [AH 141], a phenylpropanone derivative, is presently classified as a class Ic antiarrhythmic agent, it is a sodium channel antagonist. Alprafenone's range of actions is consistent with that of other effective antiarrhythmic drugs and is very similar to that of propafenone. Alprafenone was under preclinical development with Helopharm (Germany), but later this development was discontinued.
Originator
Approval Year
Sample Use Guides
In canine Purkinje fibers (PF) with normal maximum diastolic potentials (MDPs), alprafenone (5 x 10(-8)-1 x 10(-6) M) produced concentration-dependent decreases in AP amplitude (APA), Vmax, AP duration (APD), and conduction velocity. Alprafenone produced a reduction in contraction amplitude of rat electrically stimulated myocytes with a similar dose-response relationship (IC50 approx. 10 umol/l).
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C47793
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6509
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C076009
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SUB05369MIG
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65951
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100000087452
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D5H25D039V
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ACTIVE MOIETY