Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H15N3O3S |
| Molecular Weight | 281.331 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1CC=NN1C(=O)NS(=O)(=O)C2=CC=C(C)C=C2
InChI
InChIKey=OUUYOZGHNAGYNC-UHFFFAOYSA-N
InChI=1S/C12H15N3O3S/c1-9-3-5-11(6-4-9)19(17,18)14-12(16)15-10(2)7-8-13-15/h3-6,8,10H,7H2,1-2H3,(H,14,16)
| Molecular Formula | C12H15N3O3S |
| Molecular Weight | 281.331 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Glipalamide (Glipolamid) is a hypoglycemic agent and part of the second-generation sulfonamide derivatives. These sulphonylureas are used as medication to control blood sugar levels in patients with diabetes type 2. Like other sulphonylureas, glipalamide exerts extra-pancreatic activity. The antihyperglycemic action of this compound (and other sulphonylureas) may be explained by increased affinity of insulin receptors and the stimulating action of these compounds on peripheral glucose metabolism. Glipalamide was analyzed for its physical-chemical properties. After oral administration in animals, no differences were observed in insulin concentration between experimental and control groups, despite a significant fall in blood glucose level.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:58:58 GMT 2025
by
admin
on
Mon Mar 31 17:58:58 GMT 2025
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| Record UNII |
W7J490CUHM
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C97936
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65802
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W7J490CUHM
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6496
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CHEMBL2105149
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SUB07926MIG
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DTXSID80865876
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37598-94-0
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C72797
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100000084222
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PRIMARY |
| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |