Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H4O5S.H2O |
| Molecular Weight | 158.13 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.OC(=O)CS(O)(=O)=O
InChI
InChIKey=IWPVKNZTNOPDLI-UHFFFAOYSA-N
InChI=1S/C2H4O5S.H2O/c3-2(4)1-8(5,6)7;/h1H2,(H,3,4)(H,5,6,7);1H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Sulfoacetate is degraded via a novel pathway involving sulfoacetyl-CoA and sulfoacetaldehyde in Cupriavidus necator H16. | 2010-11-12 |
|
| Sulfoacetate released during the assimilation of taurine-nitrogen by Neptuniibacter caesariensis: purification of sulfoacetaldehyde dehydrogenase. | 2008-08 |
|
| Differential inhibition of cytosolic PEPCK by substrate analogues. Kinetic and structural characterization of inhibitor recognition. | 2008-02-19 |
|
| The DUF81 protein TauE in Cupriavidus necator H16, a sulfite exporter in the metabolism of C2 sulfonates. | 2007-09 |
|
| Sulfoacetaldehyde is excreted quantitatively by Acinetobacter calcoaceticus SW1 during growth with taurine as sole source of nitrogen. | 2005-04 |
|
| Sulfoacetate generated by Rhodopseudomonas palustris from taurine. | 2004-10 |
|
| Rheological properties of sulfoacetate derivatives of cellulose. | 2003-04-04 |
|
| Preparation of sulfoacetate derivatives of cellulose by direct esterification. | 2003-04-04 |
|
| Ethanedisulfonate is degraded via sulfoacetaldehyde in Ralstonia sp. strain EDS1. | 2001-07 |
|
| Pyrophosphate analogues as inhibitors of herpes simplex virus type 1 DNA polymerase. | 1980-03-28 |
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6155-83-5
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2P8287IJQ7
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20112241
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DTXSID70210538
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m10353
Created by
admin on Mon Mar 31 21:41:15 GMT 2025 , Edited by admin on Mon Mar 31 21:41:15 GMT 2025
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PRIMARY | Merck Index |
SUBSTANCE RECORD
