Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H16N2O5S |
| Molecular Weight | 300.331 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)C(O)=O
InChI
InChIKey=GCMVATDSSHTCOS-UHFFFAOYSA-N
InChI=1S/C12H16N2O5S/c1-2-3-8-13-12(17)14-20(18,19)10-6-4-9(5-7-10)11(15)16/h4-7H,2-3,8H2,1H3,(H,15,16)(H2,13,14,17)
| Molecular Formula | C12H16N2O5S |
| Molecular Weight | 300.331 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Comparative metabolism of tolbutamide by isolated hepatocytes from rat, rabbit, dog, and squirrel monkey. | 1984-03-01 |
|
| Characterization of protein kinases from bovine parotid glands. The effect of tolbutamide and its derivative on these partially purified enzymes. | 1976-03-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:35:35 GMT 2025
by
admin
on
Mon Mar 31 22:35:35 GMT 2025
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| Record UNII |
JGR4FM80VY
|
| Record Status |
Validated (UNII)
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| Record Version |
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JGR4FM80VY
Created by
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2224-10-4
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DTXSID10176780
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admin on Mon Mar 31 22:35:35 GMT 2025 , Edited by admin on Mon Mar 31 22:35:35 GMT 2025
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159651
Created by
admin on Mon Mar 31 22:35:35 GMT 2025 , Edited by admin on Mon Mar 31 22:35:35 GMT 2025
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