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Details

Stereochemistry RACEMIC
Molecular Formula C16H13ClN2O4S
Molecular Weight 364.803
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SUCLOFENIDE

SMILES

NS(=O)(=O)C1=CC(Cl)=C(C=C1)N2C(=O)CC(C2=O)C3=CC=CC=C3

InChI

InChIKey=JUIHCCIFJCSFON-UHFFFAOYSA-N
InChI=1S/C16H13ClN2O4S/c17-13-8-11(24(18,22)23)6-7-14(13)19-15(20)9-12(16(19)21)10-4-2-1-3-5-10/h1-8,12H,9H2,(H2,18,22,23)

HIDE SMILES / InChI

Molecular Formula C16H13ClN2O4S
Molecular Weight 364.803
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Suclofenide is a benzenesulfonamide derivative patented by Geistlich, Ed., Soehne A.-G. fuer Chemische Industrie as anticonvulsant and antiepileptic agent. In preclinical models Suclofenide shows potent anticonvulsant activity against electroshock- and pentylenetetrazole-induced convulsions in mice. Sublethal toxic manifestations were drowsiness, myoclonic twitches, and diarrhea.

Approval Year

PubMed

PubMed

TitleDatePubMed
3-Chloro-4-(phenylsuccinimido)-benzenesulfonamide (GS 385), a new anticonvulsant: its quantitative determination, pharmacokinetics and metabolism using high performance liquid chromatography.
1979
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:02:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:02:27 GMT 2023
Record UNII
3V0537Z59Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SUCLOFENIDE
INN   MI  
INN  
Official Name English
suclofenide [INN]
Common Name English
SUCLOFENIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID60865536
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
250-111-5
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
CAS
30279-49-3
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
PUBCHEM
72094
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
MERCK INDEX
m941
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
3833
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
ChEMBL
CHEMBL315877
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
FDA UNII
3V0537Z59Q
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
SMS_ID
100000083508
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
EVMPD
SUB10666MIG
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
NCI_THESAURUS
C72848
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
INN
4008
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
MESH
C015381
Created by admin on Fri Dec 15 18:02:27 GMT 2023 , Edited by admin on Fri Dec 15 18:02:27 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY