Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H11Cl3NO4S.Na |
| Molecular Weight | 454.687 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]C1=C(CCS(=O)(=O)C2=CC=C(Cl)C=C12)C(=O)NC3=CC=C(Cl)C(Cl)=C3
InChI
InChIKey=DBAQZKACATZPLT-UHFFFAOYSA-M
InChI=1S/C17H12Cl3NO4S.Na/c18-9-1-4-15-12(7-9)16(22)11(5-6-26(15,24)25)17(23)21-10-2-3-13(19)14(20)8-10;/h1-4,7-8,22H,5-6H2,(H,21,23);/q;+1/p-1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Amiodarone causes acute oxidant lung injury in ventilated and perfused rabbit lungs. | 1988-07 |
|
| The amplified chemiluminescence test to characterize antirheumatic drugs as oxygen radical scavengers. | 1987-04-01 |
|
| Diclofenac and enolicam as ocular anti-inflammatory drugs in rabbit corneal wound model. | 1986 |
|
| Inhibitors of lipoxygenase products improve survival in traumatic shock. | 1984-10 |
|
| A new model of osteoarthritis in rabbits. II. Evaluation of anti-osteoarthritic effects of selected antirheumatic drugs administered systemically. | 1983-09 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
300000055465
Created by
admin on Mon Mar 31 21:24:21 GMT 2025 , Edited by admin on Mon Mar 31 21:24:21 GMT 2025
|
PRIMARY | |||
|
VKD61J0J01
Created by
admin on Mon Mar 31 21:24:21 GMT 2025 , Edited by admin on Mon Mar 31 21:24:21 GMT 2025
|
PRIMARY | |||
|
23677876
Created by
admin on Mon Mar 31 21:24:21 GMT 2025 , Edited by admin on Mon Mar 31 21:24:21 GMT 2025
|
PRIMARY | |||
|
59756-39-7
Created by
admin on Mon Mar 31 21:24:21 GMT 2025 , Edited by admin on Mon Mar 31 21:24:21 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
