Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H24N2O2.ClH |
| Molecular Weight | 312.835 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC1=CC=CC(C)=C1NC(=O)C2CCCCN2CCO
InChI
InChIKey=ZBNGGCXOSMHCEV-UHFFFAOYSA-N
InChI=1S/C16H24N2O2.ClH/c1-12-6-5-7-13(2)15(12)17-16(20)14-8-3-4-9-18(14)10-11-19;/h5-7,14,19H,3-4,8-11H2,1-2H3,(H,17,20);1H
| Molecular Formula | C16H24N2O2 |
| Molecular Weight | 276.374 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Droxicainide is a new antiarrhythmic agent. When given intravenously droxicainide suppressed ouabain-induced arrhythmias in pentobarbital-anesthetized guinea pigs. The initial experimental studies reported that droxicainide appears to have a more potent antiarrhythmic activity and fewer side effects than lidocaine. In local anesthetic tests and following intradermal administration to rabbits, droxicainide produced less local tissue irritation than lidocaine. Droxicainide is a class 1 anti-arrhythmic drug.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:46:31 GMT 2023
by
admin
on
Sat Dec 16 09:46:31 GMT 2023
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| Record UNII |
91801A0812
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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149572-05-4
Created by
admin on Sat Dec 16 09:46:31 GMT 2023 , Edited by admin on Sat Dec 16 09:46:31 GMT 2023
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3060807
Created by
admin on Sat Dec 16 09:46:31 GMT 2023 , Edited by admin on Sat Dec 16 09:46:31 GMT 2023
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91801A0812
Created by
admin on Sat Dec 16 09:46:31 GMT 2023 , Edited by admin on Sat Dec 16 09:46:31 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
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