Details
Stereochemistry | RACEMIC |
Molecular Formula | C12H14N2O3 |
Molecular Weight | 234.2512 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC2=CC=CC=C2C(=O)N1CC(O)CO
InChI
InChIKey=NTGLQWGMESPVBV-UHFFFAOYSA-N
InChI=1S/C12H14N2O3/c1-8-13-11-5-3-2-4-10(11)12(17)14(8)6-9(16)7-15/h2-5,9,15-16H,6-7H2,1H3
Molecular Formula | C12H14N2O3 |
Molecular Weight | 234.2512 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Diproqualone was used primarily for the treatment of inflammatory pain associated with osteoarthritis. The analgesic activity of diproqualoneis synergistic with that of noramidopyrine. It also display anti-inflammatory action in the rat, inhibiting plantar edema with dextran or serotonin, atopic edema from ovalbumin, etc. It has spasmolytic, anticholinergic and antihistaminic action in higher doses. It is not hypnotic and has no anticonvulsant effects. The therapeutic symptoms for diproqualone are all types of pain: postoperative, posttraumatic, dental, neuritis, anti-inflammatory arthritis, etc.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:04:38 GMT 2023
by
admin
on
Fri Dec 15 16:04:38 GMT 2023
|
Record UNII |
QY7HLH8V4L
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C241
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
SUB07226MIG
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
100000082354
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
Diproqualone
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
36518-02-2
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
64112
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
2737
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
253-081-1
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
CHEMBL2106200
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
QY7HLH8V4L
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
DTXSID30865821
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY | |||
|
C65433
Created by
admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |