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(F)=CC=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 |
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Enhancement of working memory performance in the rat by MDL 26,479, a novel compound with activity at the GABAA receptor complex. | 1992 Jan 8 |
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Traumatic brain injury and the effects of diazepam, diltiazem, and MK-801 on GABA-A receptor subunit expression in rat hippocampus. | 2010 May 18 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:32:16 GMT 2023
by
admin
on
Fri Dec 15 15:32:16 GMT 2023
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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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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 |