Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H8N4O4S2 |
| Molecular Weight | 240.261 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=S1(=O)N2CN3CN1CN(C2)S3(=O)=O
InChI
InChIKey=AGGKEGLBGGJEBZ-UHFFFAOYSA-N
InChI=1S/C4H8N4O4S2/c9-13(10)5-1-6-3-8(13)4-7(2-5)14(6,11)12/h1-4H2
| Molecular Formula | C4H8N4O4S2 |
| Molecular Weight | 240.261 |
| 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 |
|---|---|---|
| Combined diazepam and MK-801 therapy provides synergistic protection from tetramethylenedisulfotetramine-induced tonic-clonic seizures and lethality in mice. | 2015-05 |
|
| Post-exposure administration of diazepam combined with soluble epoxide hydrolase inhibition stops seizures and modulates neuroinflammation in a murine model of acute TETS intoxication. | 2014-12-01 |
|
| Tetramethylenedisulfotetramine alters Ca²⁺ dynamics in cultured hippocampal neurons: mitigation by NMDA receptor blockade and GABA(A) receptor-positive modulation. | 2012-12 |
|
| Differential antagonism of tetramethylenedisulfotetramine-induced seizures by agents acting at NMDA and GABA(A) receptors. | 2012-11-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:52:58 GMT 2025
by
admin
on
Mon Mar 31 22:52:58 GMT 2025
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| Record UNII |
F6TS3WME05
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| Record Status |
Validated (UNII)
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| Record Version |
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F6TS3WME05
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80-12-6
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64148
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m10644
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172824
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DTXSID8040307
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Tetramethylenedisulfotetramine
Created by
admin on Mon Mar 31 22:52:58 GMT 2025 , Edited by admin on Mon Mar 31 22:52:58 GMT 2025
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