99-14-9
Chemical Structure
Tricarballylic acid
- CAS No.: 99-14-9
- Formula:C6H8O6
- Molecular Weight:176.12
IUPAC Name: propane-1,2,3-tricarboxylic acid
InChIKey: KQTIIICEAUMSDG-UHFFFAOYSA-N
SMILES: O=C(CC(C(O)=O)CC(O)=O)O
Biological Activity: Tricarballylic acid is an orally active compound that can be produced by rumen microorganisms and has the activity of chelating magnesium. Tricarballylic acid is also a competitive inhibitor of aconitate hydratase, with a Ki value of 0.52 mM. Tricarballylic acid can inhibit the oxidation of acetate in the citric acid cycle and can be used in the research of ruminant tissue metabolism and grass tetany syndrome. In addition, Tricarballylic acid can be used to synthesize specific complexes and produce plasticizers[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Tricarballylic acid | 98.0% | Tricarballylic acid is an orally active compound that can be produced by rumen microorganisms and has the activity of chelating magnesium. Tricarballylic acid is also a competitive inhibitor of aconitate hydratase, with a Ki value of 0.52 mM. Tricarballylic acid can inhibit the oxidation of acetate in the citric acid cycle and can be used in the research of ruminant tissue metabolism and grass tetany syndrome. In addition, Tricarballylic acid can be used to synthesize specific complexes and produce plasticizers. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Tricarballylic acid (Standard) | 99.97% | Tricarballylic acid (Standard) is the analytical standard of Tricarballylic acid (HY-W020215). This product is intended for research and analytical applications. Tricarballylic acid is an orally active compound that can be produced by rumen microorganisms and has the activity of chelating magnesium. Tricarballylic acid is also a competitive inhibitor of aconitate hydratase, with a Ki value of 0.52 mM. Tricarballylic acid can inhibit the oxidation of acetate in the citric acid cycle and can be used in the research of ruminant tissue metabolism and grass tetany syndrome. In addition, Tricarballylic acid can be used to synthesize specific complexes and produce plasticizers. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
-
Similarity Score 0.82
HY-113410R3-Methylglutaric acid (Standard) -
Similarity Score 0.82
HY-W007752R3-Oxopentanedioic acid (Standard) -
Similarity Score 0.81
HY-W7184183-Ketoadipic acid -
Similarity Score 0.80
HY-164728Pregabalin diacid -
Similarity Score 0.78
HY-1132773-Methyladipic acid -
Similarity Score 0.78
HY-N157543-Hydroxy-2-methylglutaric acid -
Similarity Score 0.78
HY-W010381R2-Methylsuccinic acid (Standard) -
Similarity Score 0.77
HY-W018541R3-Isobutylglutaric acid (Standard) -
Similarity Score 0.77
HY-W0175242-Methylpentanedioic acid -
Explore the MedChemAI to find more analogs
References
- [1]. Russell JB, et al. Production of tricarballylic acid by rumen microorganisms and its potential toxicity in ruminant tissue metabolism. Br J Nutr. 1986 Jul;56(1):153-62. [Content Brief]
- [2]. Schwartz R, et al. Effect of tricarballylic acid, a nonmetabolizable rumen fermentation product of trans-aconitic acid, on Mg, Ca and Zn utilization of rats. J Nutr. 1988 Feb;118(2):183-8. [Content Brief]
- [3]. Vlahou I, et al. Zinc complexes with tricarballylic acid and Lewis bases with zero-and two-dimensional structures. Inorganica chimica acta, 2006, 359(11): 3540-3548.
- [4]. Magne F C, et al. Plasticizers from aconitic and tricarballylic acids. Industrial & Engineering Chemistry, 1953, 45(7): 1546-1547.
