Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | O5S2 |
| Molecular Weight | 144.127 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | -2 |
SHOW SMILES / InChI
SMILES
[O-]S(=O)S([O-])(=O)=O
InChI
InChIKey=WBZKQQHYRPRKNJ-UHFFFAOYSA-L
InChI=1S/H2O5S2/c1-6(2)7(3,4)5/h(H,1,2)(H,3,4,5)/p-2
| Molecular Formula | H2O5S2 |
| Molecular Weight | 146.143 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25463229
The purpose of the study was to investigate the effect of sodium metabisulfite (SMB) on the expression of big-conductance Ca(2+)-activated K(+) (BKCa), ATP-sensitive K(+) (KATP), and L-type calcium (L-Ca(2+)) channels in rat aorta in vivo and in vitro. The results showed that the mRNA and protein levels of the BKCa channel subunits α and β1 of the aorta in rats were increased by SMB in vivo and in vitro. Similarly, the expression of the KATP channel subunits Kir6.1, Kir6.2, and SUR2B were increased by SMB. However, SMB at the highest concentration significantly decreased the expression of the L-Ca(2+) channel subunits Cav1.2 and Cav1.3.
| Substance Class |
Chemical
Created
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Edited
Mon Mar 31 19:58:14 GMT 2025
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7992SO049K
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Validated (UNII)
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23134-05-6
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