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 | 22.98976928 |
| 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
Mon Mar 31 21:55:27 GMT 2025
by
admin
on
Mon Mar 31 21:55:27 GMT 2025
|
| Record UNII |
787WKQ2464
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID801014642
Created by
admin on Mon Mar 31 21:55:27 GMT 2025 , Edited by admin on Mon Mar 31 21:55:27 GMT 2025
|
PRIMARY | |||
|
4504-50-1
Created by
admin on Mon Mar 31 21:55:27 GMT 2025 , Edited by admin on Mon Mar 31 21:55:27 GMT 2025
|
PRIMARY | |||
|
224-817-9
Created by
admin on Mon Mar 31 21:55:27 GMT 2025 , Edited by admin on Mon Mar 31 21:55:27 GMT 2025
|
PRIMARY | |||
|
787WKQ2464
Created by
admin on Mon Mar 31 21:55:27 GMT 2025 , Edited by admin on Mon Mar 31 21:55:27 GMT 2025
|
PRIMARY | |||
|
165240
Created by
admin on Mon Mar 31 21:55:27 GMT 2025 , Edited by admin on Mon Mar 31 21:55:27 GMT 2025
|
PRIMARY |