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 |
---|---|---|
Tetramethylenedisulfotetramine alters Ca²⁺ dynamics in cultured hippocampal neurons: mitigation by NMDA receptor blockade and GABA(A) receptor-positive modulation. | 2012 Dec |
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Differential antagonism of tetramethylenedisulfotetramine-induced seizures by agents acting at NMDA and GABA(A) receptors. | 2012 Nov 15 |
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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 Dec 1 |
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Combined diazepam and MK-801 therapy provides synergistic protection from tetramethylenedisulfotetramine-induced tonic-clonic seizures and lethality in mice. | 2015 May |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:52:43 GMT 2023
by
admin
on
Sat Dec 16 09:52:43 GMT 2023
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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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-
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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 Sat Dec 16 09:52:43 GMT 2023 , Edited by admin on Sat Dec 16 09:52:43 GMT 2023
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