U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H11ClN2O4S
Molecular Weight 278.713
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JNJ-26489112

SMILES

NS(=O)(=O)NC[C@H]1COC2=C(O1)C=CC(Cl)=C2

InChI

InChIKey=KXSAIQPPGSSNKX-ZETCQYMHSA-N
InChI=1S/C9H11ClN2O4S/c10-6-1-2-8-9(3-6)15-5-7(16-8)4-12-17(11,13)14/h1-3,7,12H,4-5H2,(H2,11,13,14)/t7-/m0/s1

HIDE SMILES / InChI

Approval Year

Name Type Language
JNJ-26489112
Code English
SULFAMIDE, N-(((2S)-6-CHLORO-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL)METHYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
11616111
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
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CAS
871824-55-4
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
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WIKIPEDIA
JNJ-26489112
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
PRIMARY JNJ-26489112 is an anticonvulsant drug being developed by Johnson & Johnson for the treatment of epilepsy. JNJ-26489112 was designed as a successor to topiramate. It is expected to have fewer side effects than topiramate because it lacks activity against carbonic anhydrase. JNJ-26489112 is also being studied as a treatment for major depressive disorder.
DRUG BANK
DB15203
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID601031470
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
PRIMARY
FDA UNII
G1TI012DLT
Created by admin on Sat Dec 16 05:14:41 GMT 2023 , Edited by admin on Sat Dec 16 05:14:41 GMT 2023
PRIMARY