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Details

Stereochemistry RACEMIC
Molecular Formula C24H28N4O7S
Molecular Weight 516.567
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NS-1209, (±)-

SMILES

CN(C)S(=O)(=O)C1=CC=C(C=C1)C2=CC3=C(NC(=O)\C3=N/OC(CCO)C(O)=O)C4=C2CCN(C)C4

InChI

InChIKey=CFJRSKULEDUDKL-UHFFFAOYSA-N
InChI=1S/C24H28N4O7S/c1-27(2)36(33,34)15-6-4-14(5-7-15)17-12-18-21(19-13-28(3)10-8-16(17)19)25-23(30)22(18)26-35-20(9-11-29)24(31)32/h4-7,12,20,29H,8-11,13H2,1-3H3,(H,31,32)(H,25,26,30)

HIDE SMILES / InChI

Molecular Formula C24H28N4O7S
Molecular Weight 516.567
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Modifications of antiepileptic drugs for improved tolerability and efficacy.
2008-02-14
Behavioural effects of the novel AMPA/GluR5 selective receptor antagonist NS1209 after systemic administration in animal models of experimental pain.
2004-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:17:53 GMT 2025
Edited
by admin
on Mon Mar 31 21:17:53 GMT 2025
Record UNII
X607LN281T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NS-1209, (±)-
Common Name English
(RS)-NS-1209
Preferred Name English
NS-1209, (RS)-
Common Name English
2-(((5-(4-((DIMETHYLAMINO)SULFONYL)PHENYL)-1,2,6,7,8,9-HEXAHYDRO-8-METHYL-2-OXO-3H-PYRROLO(3,2-H)ISOQUINOLIN-3-YLIDENE)AMINO)OXY)-4-HYDROXYBUTANOIC ACID
Systematic Name English
SPD-502
Common Name English
BUTANOIC ACID, 2-(((5-(4-((DIMETHYLAMINO)SULFONYL)PHENYL)-1,2,6,7,8,9-HEXAHYDRO-8-METHYL-2-OXO-3H-PYRROLO(3,2-H)ISOQUINOLIN-3-YLIDENE)AMINO)OXY)-4-HYDROXY-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID70948364
Created by admin on Mon Mar 31 21:17:53 GMT 2025 , Edited by admin on Mon Mar 31 21:17:53 GMT 2025
PRIMARY
CAS
254751-28-5
Created by admin on Mon Mar 31 21:17:53 GMT 2025 , Edited by admin on Mon Mar 31 21:17:53 GMT 2025
SUPERSEDED
CAS
245063-59-6
Created by admin on Mon Mar 31 21:17:53 GMT 2025 , Edited by admin on Mon Mar 31 21:17:53 GMT 2025
PRIMARY
FDA UNII
X607LN281T
Created by admin on Mon Mar 31 21:17:53 GMT 2025 , Edited by admin on Mon Mar 31 21:17:53 GMT 2025
PRIMARY
PUBCHEM
135413541
Created by admin on Mon Mar 31 21:17:53 GMT 2025 , Edited by admin on Mon Mar 31 21:17:53 GMT 2025
PRIMARY