Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H22N4 |
Molecular Weight | 258.362 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCN1C2=CC=CC=C2N3CCN=C13
InChI
InChIKey=AQUZIHYIKZOILJ-UHFFFAOYSA-N
InChI=1S/C15H22N4/c1-3-17(4-2)11-12-19-14-8-6-5-7-13(14)18-10-9-16-15(18)19/h5-8H,3-4,9-12H2,1-2H3
Molecular Formula | C15H22N4 |
Molecular Weight | 258.362 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Limiglidole belongs to the class of benzimidazole derivatives exhibiting various biological activities including inhibition of platelet aggregation and prolongation of clotting time in animal models. It inhibited platelet aggregation induced by ADP. Antithrombotic activity of hypoglycemic compound limiglidole that exhibits antiplatelet activity 2-fold exceeded activity of antiplatelet agent acetylsalicylic acid in the mouse model of systemic collagen-epinephrine thrombosis. Antithrombogenic properties of limiglidole are beneficial in the treatment of diabetes mellitus.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26033587
Single dose 36 mg/kg
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:01:46 GMT 2023
by
admin
on
Fri Dec 15 16:01:46 GMT 2023
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Record UNII |
X0U1YVN4X9
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |