Sodium pyruvate

Sodium pyruvate
Ball-and-stick model of the pyruvate anion	The sodium cation
Names
	Preferred IUPAC name Sodium 2-oxopropanoate
	Other names α-Ketopropionic acid sodium salt; 2-Oxopropanoic acid sodium salt; Pyruvic acid sodium salt;
Identifiers
CAS Number	113-24-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:50144 ;
ChEMBL	ChEMBL181886 ;
ChemSpider	7931 ;
ECHA InfoCard	100.003.659
PubChem CID	23662274;
UNII	POD38AIF08 ;
CompTox Dashboard (EPA)	DTXSID6040614 ;
	InChI InChI=1S/C3H4O3.Na/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1 Key: DAEPDZWVDSPTHF-UHFFFAOYSA-M ; InChI=1/C3H4O3.Na/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1 Key: DAEPDZWVDSPTHF-REWHXWOFAL;
	SMILES [Na+].[O-]C(=O)C(=O)C;
Properties
Chemical formula	C3H3NaO3
Molar mass	110.044 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Sodium pyruvate is a salt of the conjugate anion form of pyruvic acid, known as pyruvate. It is commonly added to cell culture media as an additional source of energy, but may also have protective effects against hydrogen peroxide. This was reported by Giandomenico et al.^[1] and has been confirmed by several independent groups.

Due to pyruvate being an intermediate in many pathways for metabolism including glycolysis, sodium pyruvate has been used in many experiments involving cell cultures to provide more energy. In adipocytes it was found that sodium pyruvate promoted increased uptake of insulin-mediated glucose.^[2] In the body, one way in which sodium pyruvate provides energy to cells is through pyruvate conversion to acetyl-CoA which then can enter the TCA cycle which produces energy and is linked to other energy producing processes.^[2]

Along with having antioxidant properties and energy producing effects, sodium pyruvate has the ability to cross the blood-brain barrier and is used in several studies on brain injury because of these characteristics.^[3]^[4]

References

[1]

[2]

[3]

[4]