Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H25N3O5 |
| Molecular Weight | 363.4082 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)NC1=C(OC)C2=C(OC=C2)C(OC)=C1OCCN3CCCC3
InChI
InChIKey=BWMMRMDCODVQBX-UHFFFAOYSA-N
InChI=1S/C18H25N3O5/c1-19-18(22)20-13-14(23-2)12-6-10-25-15(12)17(24-3)16(13)26-11-9-21-7-4-5-8-21/h6,10H,4-5,7-9,11H2,1-3H3,(H2,19,20,22)
| Molecular Formula | C18H25N3O5 |
| Molecular Weight | 363.4082 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Carocainide is a benzofuran derivative patented by pharmaceutical company Delalande S. A. For treatment cardiovascular disease. Carocainide showing antiarrhythmic properties in animal models. In isolated papillary muscles and Purkinje fibers it decreases the maximum rate of rise of the action potential and in Purkinje fibers it decreases the plateau amplitude and the duration of the action potential. Carocainide increases the ratio of the effective refractory period to the action potential duration at 90% of repolarization, shifts the membrane responsiveness curve towards more negative membrane potentials and slows down the recovery of the maximum rate of rise of the action potentials of the Purkinje fibers. Carocainide also increases the conduction time at the Purkinje papillary muscle junction.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2467080
3.5 mg/kg
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:28:47 GMT 2025
by
admin
on
Wed Apr 02 08:28:47 GMT 2025
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| Record UNII |
T643E80J9K
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English |
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NCI_THESAURUS |
C47793
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C038839
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DTXSID00216381
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |