Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H8ClNO3 |
| Molecular Weight | 225.628 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC2=C(OC3CCON3C2=O)C=C1
InChI
InChIKey=XWXVKXXKKLBDDJ-UHFFFAOYSA-N
InChI=1S/C10H8ClNO3/c11-6-1-2-8-7(5-6)10(13)12-9(15-8)3-4-14-12/h1-2,5,9H,3-4H2
| Molecular Formula | C10H8ClNO3 |
| Molecular Weight | 225.628 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/4761775
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4761775
Seclazone was developed as a non-steroidal anti-inflammatory agent. This compound also possesses analgesic and antipyretic properties. Information about the current use of this compound is not available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Optimal conditions for the hydrolysis of seclazone by rat hepatic microsomes. | 1974-09 |
|
| The metabolic fate of seclazone in man. | 1974-05 |
|
| The pharmacological properties of seclazone (7-chloro-3,3a-dihydro-2H, 9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one) a new anti-inflammatory agent. | 1973 |
|
| The in vivo antibradykinin activity of seclazone (7-chloro-3,3a-dihydro-2H,9H-isoxazolo(3,2-b) (1,3)benzoxazin-9-one), a new anti-inflammatory agent. | 1973 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:07:10 GMT 2025
by
admin
on
Wed Apr 02 09:07:10 GMT 2025
|
| Record UNII |
JW3UZ4I1A8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C921
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C73105
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
DTXSID10865465
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
29050-11-1
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
3239
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
JW3UZ4I1A8
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
CHEMBL2105593
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
294833
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
100000084103
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
34443
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
SUB10466MIG
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY | |||
|
C067602
Created by
admin on Wed Apr 02 09:07:10 GMT 2025 , Edited by admin on Wed Apr 02 09:07:10 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |