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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H10N2O2S2
Molecular Weight 242.318
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JNJ-26990990

SMILES

NS(=O)(=O)NCC1=CSC2=CC=CC=C12

InChI

InChIKey=AWSKBQNOSRREEY-UHFFFAOYSA-N
InChI=1S/C9H10N2O2S2/c10-15(12,13)11-5-7-6-14-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H2,10,12,13)

HIDE SMILES / InChI

Molecular Formula C9H10N2O2S2
Molecular Weight 242.318
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
48.0 µM [IC50]
Target ID: Q00975
Gene ID: 774.0
Gene Symbol: CACNA1B
Target Organism: Homo sapiens (Human)
28.0 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Novel, broad-spectrum anticonvulsants containing a sulfamide group: advancement of N-((benzo[b]thien-3-yl)methyl)sulfamide (JNJ-26990990) into human clinical studies.
2009-12-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:31:45 GMT 2025
Edited
by admin
on Mon Mar 31 22:31:45 GMT 2025
Record UNII
QFG58Y96EP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-((BENZO(B)THIEN-3-YL)METHYL)SULFAMIDE
Preferred Name English
JNJ-26990990
Common Name English
SULFAMIDE, (BENZO(B)THIEN-3-YLMETHYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
11687376
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
SMS_ID
300000051565
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
FDA UNII
QFG58Y96EP
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
WIKIPEDIA
JNJ-26990990
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
CAS
877316-38-6
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID20470625
Created by admin on Mon Mar 31 22:31:45 GMT 2025 , Edited by admin on Mon Mar 31 22:31:45 GMT 2025
PRIMARY
Related Record Type Details
METABOLITE -> PARENT
MAJOR
URINE
Related Record Type Details
ACTIVE MOIETY