Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H12N2O4S |
| Molecular Weight | 280.3 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1N(C2CCCNC2=O)S(=O)(=O)C3=CC=CC=C13
InChI
InChIKey=QQWLXNMPPFCVCD-UHFFFAOYSA-N
InChI=1S/C12H12N2O4S/c15-11-9(5-3-7-13-11)14-12(16)8-4-1-2-6-10(8)19(14,17)18/h1-2,4,6,9H,3,5,7H2,(H,13,15)
| Molecular Formula | C12H12N2O4S |
| Molecular Weight | 280.3 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Supidimide is a benzisothiazol derivative patented by Chemie Gruenenthal G.m.b.H. as a sedative and hypnotic agent. Supidimide acts as serotonin release inhibitor and decreases of 5-HT release into the synaptic cleft in preclinical studies. In clinical trials, Supidimide substantially relieved sleep disturbances in schizophrenic inpatients. Besides that Supidimide administration associated with a decrease in "somatic concern", items related to agitation, "irritability" and "manifest psychosis", and a slight increase in "retardation".
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Non-steroidal anti-inflammatory drugs stimulate secretion of non-amyloidogenic precursor protein. | 2002-08-30 |
|
| Thalidomide impairment of trinitrobenzene sulphonic acid-induced colitis in the rat - role of endothelial cell-leukocyte interaction. | 2001-08 |
|
| The effect of thalidomide and 2 analogs on collagen induced arthritis. | 1998-05 |
|
| Effects of supidimide in schizophrenic inpatients undergoing neuroleptic maintenance therapy with haloperidol. | 1982 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7049709
2 x 200 mg per day.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:58:14 GMT 2025
by
admin
on
Mon Mar 31 17:58:14 GMT 2025
|
| Record UNII |
L2GWR3US1G
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C74382
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
49785-74-2
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
DTXSID40866142
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
C027948
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
L2GWR3US1G
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
3841
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
100000082964
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
256-490-3
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
39528
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
CHEMBL72115
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY | |||
|
SUB10775MIG
Created by
admin on Mon Mar 31 17:58:14 GMT 2025 , Edited by admin on Mon Mar 31 17:58:14 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |