Pantetheine

Pantetheine
Names
	IUPAC name 2,4-Dihydroxy-3,3-dimethyl-N-[2-(2-sulfanylethylcarbamoyl)ethyl]butanamide
	Other names Pantetheine
Identifiers
CAS Number	496-65-1 R ;
3D model (JSmol)	Interactive image;
3DMet	B00185;
Beilstein Reference	1714196 R
ChEBI	CHEBI:16753 ;
ChemSpider	466 ; 388453 R ;
ECHA InfoCard	100.007.114
EC Number	207-824-1;
KEGG	C00831 ;
MeSH	Pantetheine
PubChem CID	479; 439322 R;
UNII	VCH6X4IARE R ;
	InChI InChI=1S/C11H22N2O4S/c1-11(2,7-14)9(16)10(17)13-4-3-8(15)12-5-6-18/h9,14,16,18H,3-7H2,1-2H3,(H,12,15)(H,13,17) Key: ZNXZGRMVNNHPCA-UHFFFAOYSA-N ;
	SMILES CC(C)(CO)C(O)C(=O)NCCC(=O)NCCS;
Properties
Chemical formula	C11H22N2O4S
Molar mass	278.37 g·mol−1
Related compounds
Related compounds	Pantethine
	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

Pantetheine is the cysteamine amide analog of pantothenic acid (vitamin B₅). The dimer of this compound, pantethine is more commonly known, and is considered to be the most potent form of vitamin B₅. Pantetheine is an intermediate in the production of coenzyme A by the body.[1]

References

MB Hoagland, GD Novelli (1954). "Biosynthesis of coenzyme A from phosphopantetheine and of pantetheine from pantothenate". Journal of Biological Chemistry. 207: 767–773.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] MB Hoagland, GD Novelli (1954). "Biosynthesis of coenzyme A from phosphopantetheine and of pantetheine from pantothenate". Journal of Biological Chemistry. 207: 767–773.