Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H9N3O2 |
| Molecular Weight | 215.2081 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)N\N=C1/C=CC2=CC=CC=C2C1=O
InChI
InChIKey=TZGBBMBARSFJBG-UKTHLTGXSA-N
InChI=1S/C11H9N3O2/c12-11(16)14-13-9-6-5-7-3-1-2-4-8(7)10(9)15/h1-6H,(H3,12,14,16)/b13-9+
| Molecular Formula | C11H9N3O2 |
| Molecular Weight | 215.2081 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Naftazone is a naphtoquinone derivative which was originally registered in several European countries for treating symptoms of varicose veins and venous insufficiency, based on its venoconstrictive properties. ts venotonic mechanism of action remains unknown, but the drug has anti‐inflammatory effects and inhibits platelet aggregation. Naftazone is shown to accelerate human saphenous vein endothelial cell proliferation in vitro at concentrations which did not alter the hemostatic balance. Naftazone, which exhibits glutamate release inhibition properties, has shown antiparkinsonian and antidyskinetic activity in preclinical models of Parkinson's disease and in a clinical proof of concept study. Naftazone is currently marketed in several countries.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:25:15 GMT 2025
by
admin
on
Wed Apr 02 09:25:15 GMT 2025
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| Record UNII |
15B0523P5L
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C78311
Created by
admin on Wed Apr 02 09:25:15 GMT 2025 , Edited by admin on Wed Apr 02 09:25:15 GMT 2025
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WHO-VATC |
QC05CX02
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WHO-ATC |
C05CX02
Created by
admin on Wed Apr 02 09:25:15 GMT 2025 , Edited by admin on Wed Apr 02 09:25:15 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DB13680
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31475
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1871
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100000084437
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DTXSID001043136
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SUB09129MIG
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239-785-1
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15B0523P5L
Created by
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CHEMBL2106794
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C90857
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5775429
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m7749
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2149
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15687-37-3
Created by
admin on Wed Apr 02 09:25:15 GMT 2025 , Edited by admin on Wed Apr 02 09:25:15 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |