Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H4O6.2Na |
Molecular Weight | 194.0505 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].O[C@@H]([C@@H](O)C([O-])=O)C([O-])=O
InChI
InChIKey=HELHAJAZNSDZJO-BZMHZNRSSA-L
InChI=1S/C4H6O6.2Na/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);;/q;2*+1/p-2/t1-,2+;;
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C4H4O6 |
Molecular Weight | 148.071 |
Charge | -2 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/23391306Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/3198841 | https://www.ncbi.nlm.nih.gov/pubmed/24906784
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23391306
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/3198841 | https://www.ncbi.nlm.nih.gov/pubmed/24906784
Mesotartaric acid is one of an isomer of Tartaric acid. Mesotartaric acid is a diastereomer which has two opposite chiral centers in the same molecule making the molecule optically inactive. Mesotartaric acid is also commonly called pyrotartaric acid because it is formed by heating d-(-)-tartaric acid. Mesotartaric Acid have several industrial application and may be used as pH regulator, a metal chelator, the reagent in organic synthesis and etc.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4460 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23391306 |
2820.0 µM [IC50] | ||
Target ID: CHEMBL5887 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23391306 |
3922.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23391306
Appropriate amounts (0.23−4.2 μg) of the purified D-aspartate oxidase was added to a reaction mixture of air-saturated 40 mM sodium pyrophosphate buffer (pH 8.3), 23 U A. niger catalase, 60 μM FAD, and 10 mM amino acids in a final volume of 150 μL. For testing the inhibitory activity of mesotartaric acid, mesotartaric acid was added to the reaction mixture. The mixture was incubated at 37 °C for 10 min, and then 10 μL of 100% (weight/vol) trichloroacetic acid was added to stop the reaction. The 2-oxo acid product was reacted with 2,4-dinitrophenylhydrazine and quantitated by measuring the A445 against a blank mixture lacking amino acids.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:10:15 GMT 2023
by
admin
on
Sat Dec 16 08:10:15 GMT 2023
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Record UNII |
787WKQ2464
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Record Status |
Validated (UNII)
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Record Version |
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