Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | H2O4S.H4N2 |
| Molecular Weight | 130.124 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NN.OS(O)(=O)=O
InChI
InChIKey=ZGCHATBSUIJLRL-UHFFFAOYSA-N
InChI=1S/H4N2.H2O4S/c1-2;1-5(2,3)4/h1-2H2;(H2,1,2,3,4)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular mechanism of anaerobic ammonium oxidation. | 2011-10-02 |
|
| Small-molecule activators of AMP-activated protein kinase (AMPK), RSVA314 and RSVA405, inhibit adipogenesis. | 2011-04-29 |
|
| Carbamoylating chemoresistance induced by cobalt pretreatment in C6 glioma cells: putative roles of hypoxia-inducible factor-1. | 2004-03 |
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C1935
Created by
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NCI_THESAURUS |
C667
Created by
admin on Mon Mar 31 17:47:16 GMT 2025 , Edited by admin on Mon Mar 31 17:47:16 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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HYDRAZINE SULFATE
Created by
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PRIMARY | |||
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10034-93-2
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PRIMARY | |||
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C1129
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5086
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SUB32903
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PRIMARY | |||
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1N369SAT01
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150014
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100000126020
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m6080
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admin on Mon Mar 31 17:47:16 GMT 2025 , Edited by admin on Mon Mar 31 17:47:16 GMT 2025
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PRIMARY | Merck Index | ||
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233-110-4
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DTXSID8020703
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215190
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24842
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C029424
Created by
admin on Mon Mar 31 17:47:16 GMT 2025 , Edited by admin on Mon Mar 31 17:47:16 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
