Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H10NO2S2.H4N |
Molecular Weight | 198.307 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[NH4+].OCCN(CCO)C([S-])=S
InChI
InChIKey=AEALMZFAWWJXJP-UHFFFAOYSA-N
InChI=1S/C5H11NO2S2.H3N/c7-3-1-6(2-4-8)5(9)10;/h7-8H,1-4H2,(H,9,10);1H3
Molecular Formula | C5H10NO2S2 |
Molecular Weight | 180.268 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H4N |
Molecular Weight | 18.0385 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Cytochrome P450 catalyzed oxidation of monochlorobenzene, 1,2- and 1,4-dichlorobenzene in rat, mouse, and human liver microsomes. | 1998 Aug 14 |
|
Neural overexcitation and implication of NMDA and AMPA receptors in a mouse model of temporal lobe epilepsy implying zinc chelation. | 2006 May |
|
SLC30A3 responds to glucose- and zinc variations in beta-cells and is critical for insulin production and in vivo glucose-metabolism during beta-cell stress. | 2009 May 25 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 12:30:45 GMT 2023
by
admin
on
Sat Dec 16 12:30:45 GMT 2023
|
Record UNII |
4G7DCD86CJ
|
Record Status |
Validated (UNII)
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Record Version |
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-
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198570
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DTXSID40226045
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75074-70-3
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admin on Sat Dec 16 12:30:45 GMT 2023 , Edited by admin on Sat Dec 16 12:30:45 GMT 2023
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4G7DCD86CJ
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admin on Sat Dec 16 12:30:45 GMT 2023 , Edited by admin on Sat Dec 16 12:30:45 GMT 2023
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278-067-2
Created by
admin on Sat Dec 16 12:30:45 GMT 2023 , Edited by admin on Sat Dec 16 12:30:45 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
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