Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H12O6 |
| Molecular Weight | 312.2736 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)OC1=CC=CC=C1C(=O)OC2OC(=O)C3=C2C=CC=C3
InChI
InChIKey=SHCYQUDTKWHARF-UHFFFAOYSA-N
InChI=1S/C17H12O6/c1-10(18)21-14-9-5-4-8-13(14)16(20)23-17-12-7-3-2-6-11(12)15(19)22-17/h2-9,17H,1H3
Talosalate, a phthalidyl ester of acetylsalicylic acid, was used as an analgesic and anti-inflammatory agent. Talosalate was studied in preclinical experiments for the treatment of inflammation and rheumatic disorder in Argentina. However, the further development of the drug appears to have been discontinued.
Originator
Approval Year
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C257
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
SUB10812MIG
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
68558
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
4747
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
100000083227
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
CHEMBL2107476
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
C76814
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
66898-60-0
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
1356SD6O2G
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY | |||
|
DTXSID20867253
Created by
admin on Mon Mar 31 18:31:35 GMT 2025 , Edited by admin on Mon Mar 31 18:31:35 GMT 2025
|
PRIMARY |
ACTIVE MOIETY