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
Fri Dec 15 15:29:37 GMT 2023
by
admin
on
Fri Dec 15 15:29:37 GMT 2023
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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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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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37598-94-0
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C72797
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100000084222
Created by
admin on Fri Dec 15 15:29:37 GMT 2023 , Edited by admin on Fri Dec 15 15:29:37 GMT 2023
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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 |