Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H31N3O3S |
| Molecular Weight | 369.522 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCNC(=O)N(CCS(=O)(=O)C1=CC=CC=C1)C(C)C
InChI
InChIKey=OSTGVQSWUXGHKL-UHFFFAOYSA-N
InChI=1S/C18H31N3O3S/c1-5-20(6-2)13-12-19-18(22)21(16(3)4)14-15-25(23,24)17-10-8-7-9-11-17/h7-11,16H,5-6,12-15H2,1-4H3,(H,19,22)
| Molecular Formula | C18H31N3O3S |
| Molecular Weight | 369.522 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Suricainide (also known as AHR 10718) is an aminoalkylurea derivative patented by A. H. Robins Co., Inc. as an antiarrhythmic agent. Suricainide induces a use-dependent decrease in Vmax and significantly decreased Purkinje fiber conduction velocity and action potential duration. Suricainide had no effect on slow response action potentials induced by isoproterenol but ventricular muscle action potentials were significantly prolonged by Suricainide. Suricainide significantly decreased normal automaticity, catecholamine-enhanced automaticity, and abnormal automaticity induced by barium or myocardial infarction. In preclinical modes, Suricainide suppresses the aconitine-induced canine atrial arrhythmia.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3838726
Dog 10 mg/kg
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:51:05 GMT 2025
by
admin
on
Mon Mar 31 18:51:05 GMT 2025
|
| Record UNII |
28G77G373X
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C47793
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
55304
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
SUB10781MIG
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
5929
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110719
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
85053-46-9
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
DTXSID101005424
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
100000082967
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
C152477
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY | |||
|
28G77G373X
Created by
admin on Mon Mar 31 18:51:05 GMT 2025 , Edited by admin on Mon Mar 31 18:51:05 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |