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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
Structure of SUPIDIMIDE

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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

2 x 200 mg per day.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:58:14 GMT 2025
Edited
by admin
on Mon Mar 31 17:58:14 GMT 2025
Record UNII
L2GWR3US1G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SUPIDIMIDE
INN  
INN  
Official Name English
supidimide [INN]
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
NCI_THESAURUS
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
CAS
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
EPA CompTox
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
MESH
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
FDA UNII
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
INN
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
SMS_ID
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
ECHA (EC/EINECS)
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
PUBCHEM
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
ChEMBL
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
EVMPD
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