Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H10FN3S |
| Molecular Weight | 223.27 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1N=C(N(C)C1=S)C2=CC=CC(F)=C2
InChI
InChIKey=IWDUZEHNLHFBRZ-UHFFFAOYSA-N
InChI=1S/C10H10FN3S/c1-13-9(12-14(2)10(13)15)7-4-3-5-8(11)6-7/h3-6H,1-2H3
| Molecular Formula | C10H10FN3S |
| Molecular Weight | 223.27 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Suritozole (also known as MDL 26,479) is an aryldialkyltriazolethione derivative patented by Merrell Dow Pharmaceuticals, Inc as an antidepressant. Suritozole acts as negative modulator at the gamma-aminobutyric acid A (GABAA) receptor that enhances cholinergic function. In preclinical models, chronic treatment Suritozole produces a small but significant decrease in the average spontaneous firing rate of Purkinje neurons. Suritozole attenuated a scopolamine-induced acquisition deficit in a T-maze reinforced alternation task, suggesting that the compound may have memory enhancing potential.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Traumatic brain injury and the effects of diazepam, diltiazem, and MK-801 on GABA-A receptor subunit expression in rat hippocampus. | 2010-05-18 |
|
| Enhancement of working memory performance in the rat by MDL 26,479, a novel compound with activity at the GABAA receptor complex. | 1992-01-08 |
Patents
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 18:00:26 GMT 2025
by
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on
Mon Mar 31 18:00:26 GMT 2025
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| Record UNII |
3H7H68317X
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C78272
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| Code System | Code | Type | Description | ||
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C152479
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3H7H68317X
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Suritozole
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C065324
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25431
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DTXSID10149333
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SUB10783MIG
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DD-54
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100000082968
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CHEMBL278764
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7089
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110623-33-1
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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