Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H9ClN2O4S |
| Molecular Weight | 324.74 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(OC2=C1C=C(Cl)C=C2)S(=O)(=O)C3=NNC(=O)C=C3
InChI
InChIKey=FXFPQPNUMWQRAO-UHFFFAOYSA-N
InChI=1S/C13H9ClN2O4S/c1-7-9-6-8(14)2-3-10(9)20-13(7)21(18,19)12-5-4-11(17)15-16-12/h2-6H,1H3,(H,15,17)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A novel series of non-carboxylic acid, non-hydantoin inhibitors of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and congeners. | 2005-10-06 |
|
| A highly selective, non-hydantoin, non-carboxylic acid inhibitor of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran- 2-sulfonyl)-2-H-pyridazin-3-one. | 2003-06-05 |
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DB07187
Created by
admin on Mon Mar 31 21:56:01 GMT 2025 , Edited by admin on Mon Mar 31 21:56:01 GMT 2025
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U63F8E95J1
Created by
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463976-07-0
Created by
admin on Mon Mar 31 21:56:01 GMT 2025 , Edited by admin on Mon Mar 31 21:56:01 GMT 2025
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6420118
Created by
admin on Mon Mar 31 21:56:01 GMT 2025 , Edited by admin on Mon Mar 31 21:56:01 GMT 2025
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DTXSID70196828
Created by
admin on Mon Mar 31 21:56:01 GMT 2025 , Edited by admin on Mon Mar 31 21:56:01 GMT 2025
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PRIMARY |
ACTIVE MOIETY
