Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H16N2O4 |
| Molecular Weight | 276.2878 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C1=C(C)C2=C(C=C1C)C(CO)=NNC2=O
InChI
InChIKey=DUQOOLBWGUKRAJ-UHFFFAOYSA-N
InChI=1S/C14H16N2O4/c1-4-20-14(19)11-7(2)5-9-10(6-17)15-16-13(18)12(9)8(11)3/h5,17H,4,6H2,1-3H3,(H,16,18)
| Molecular Formula | C14H16N2O4 |
| Molecular Weight | 276.2878 |
| 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 |
|---|---|---|
| Long-term treatment of amyotrophic lateral sclerosis with phthalazinol. | 1992 |
|
| Role of plasma adenosine in the antiplatelet action of HL 725, a potent inhibitor of cAMP phosphodiesterase: species differences. | 1987-07-15 |
|
| Murine tumor-induced platelet aggregation and coagulation: mechanisms, inhibitors, and species differences. | 1987-04-01 |
|
| Inhibition of human and rat platelet aggregation by extracts of Mo-er (Auricularia auricula). | 1982-10-29 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:46:00 GMT 2025
by
admin
on
Mon Mar 31 17:46:00 GMT 2025
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| Record UNII |
V17MYO89WO
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C744
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C80614
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| Related Record | Type | Details | ||
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