Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H24N2O2 |
Molecular Weight | 276.374 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CC(C)=C1NC(=O)C2CCCCN2CCO
InChI
InChIKey=NVASAXNGHUPVJX-UHFFFAOYSA-N
InChI=1S/C16H24N2O2/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)
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 | ( + / - ) |
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
PubMed
Title | Date | PubMed |
---|---|---|
Pharmacological studies on droxicainide, a new antiarrhythmic agent. | 1983 |
|
Effects of lidocaine and droxicainide on myocardial necrosis: a comparative study. | 1983 Jun |
|
The acute antiarrhythmic effects of droxicainide and lidocaine in unanesthetized dogs. | 1984 Mar-Apr |
|
Comparison of electrophysiological and mechanical effects of droxicainide and lidocaine on heart muscle isolated from rats. | 1984 Oct |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6853899
2.5 mg/kg as a bolus and then as a continuous infusion for 6 hours (1.4 mg/kg).
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:27:22 GMT 2023
by
admin
on
Fri Dec 15 16:27:22 GMT 2023
|
Record UNII |
J6W196LMV3
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C47793
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
5139
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
157187
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
78289-26-6
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
78421-12-2
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
SUPERSEDED | |||
|
C72579
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
100000081028
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
SUB06418MIG
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
DTXSID20999644
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
J6W196LMV3
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
CHEMBL2106609
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY | |||
|
C038078
Created by
admin on Fri Dec 15 16:27:22 GMT 2023 , Edited by admin on Fri Dec 15 16:27:22 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |