Pantetheine

Pantetheine
Names
	Preferred IUPAC name (2R)-2,4-Dihydroxy-3,3-dimethyl-N-{3-oxo-3-[(2-sulfanylethyl)amino]propyl}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]^[2]^[3]

References

^ MB Hoagland, GD Novelli (1954). "Biosynthesis of coenzyme A from phosphopantetheine and of pantetheine from pantothenate". Journal of Biological Chemistry. 207 (2): 767–773. doi:10.1016/S0021-9258(18)65696-0. PMID 13163064.
^ Cronan, John E. (2014). "The Chain-Flipping Mechanism of ACP (Acyl Carrier Protein)-Dependent enzymes Appears Universal". Biochemical Journal. 460 (2): 157–163. doi:10.1042/BJ20140239. PMID 24825445.
^ Nitto, Takeaki; Onodera, Kenji (2013). "The Linkage Between Coenzyme a Metabolism and Inflammation: Roles of Pantetheinase". Journal of Pharmacological Sciences. 123 (1): 1–8. doi:10.1254/jphs.13R01CP. PMID 23978960.

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[1] MB Hoagland, GD Novelli (1954). "Biosynthesis of coenzyme A from phosphopantetheine and of pantetheine from pantothenate". Journal of Biological Chemistry. 207 (2): 767–773. doi:10.1016/S0021-9258(18)65696-0. PMID 13163064.

[2] Cronan, John E. (2014). "The Chain-Flipping Mechanism of ACP (Acyl Carrier Protein)-Dependent enzymes Appears Universal". Biochemical Journal. 460 (2): 157–163. doi:10.1042/BJ20140239. PMID 24825445.

[3] Nitto, Takeaki; Onodera, Kenji (2013). "The Linkage Between Coenzyme a Metabolism and Inflammation: Roles of Pantetheinase". Journal of Pharmacological Sciences. 123 (1): 1–8. doi:10.1254/jphs.13R01CP. PMID 23978960.

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