Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H7NO.C7H6O3 |
| Molecular Weight | 283.2787 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=CC=C1O.OC2=CC=CC3=CC=CN=C23
InChI
InChIKey=GOEKBPHGLUYFOX-UHFFFAOYSA-N
InChI=1S/C9H7NO.C7H6O3/c11-8-5-1-3-7-4-2-6-10-9(7)8;8-6-4-2-1-3-5(6)7(9)10/h1-6,11H;1-4,8H,(H,9,10)
| Molecular Formula | C7H6O3 |
| Molecular Weight | 138.1207 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C9H7NO |
| Molecular Weight | 145.158 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Sample Use Guides
Rabbits: oxyquinoline salicylate in dipropylene glycol (equivalent to 150 mg of the test compound) per kg. of body weight were applied to the depilated intact and abraded skin areas. Skin contact with the solution was maintained for 6 hours per day, 5 days a week, for a three-week period, and the animals were observed for two additional weeks.
Route of Administration:
Topical
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:34:08 GMT 2025
by
admin
on
Mon Mar 31 21:34:08 GMT 2025
|
| Record UNII |
98Z1AMM4PS
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DBSALT002679
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
3907
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
100000077606
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
2439-07-8
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
219-457-4
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
142766
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
DTXSID1045081
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
98Z1AMM4PS
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY | |||
|
SUB14150MIG
Created by
admin on Mon Mar 31 21:34:08 GMT 2025 , Edited by admin on Mon Mar 31 21:34:08 GMT 2025
|
PRIMARY |