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^Y
3D model (JSmol)	Interactive image
3DMet	B00185
Beilstein Reference	1714196 R
ChEBI	CHEBI:16753^N
ChemSpider	466^Y 388453 R^N
ECHA InfoCard	100.007.114
EC Number	207-824-1
KEGG	C00831^N
MeSH	Pantetheine
PubChem CID	479 439322 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)^Y Key: ZNXZGRMVNNHPCA-UHFFFAOYSA-N^Y
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).
N verify (what is ^YN ?)
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 a more potent form of vitamin B₅ than pantothenic acid. 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.

Vitamins (A11)

Fat soluble

A	α-Carotene β-Carotene Retinol^# Tretinoin
D	D₂ Ergosterol Ergocalciferol^# D₃ 7-Dehydrocholesterol Previtamin D₃ Cholecalciferol^# 25-hydroxycholecalciferol Calcitriol (1,25-dihydroxycholecalciferol) Calcitroic acid D₄ Dihydroergocalciferol D₅ D analogues Alfacalcidol Dihydrotachysterol Calcipotriol Tacalcitol Paricalcitol
E	Tocopherol Alpha Beta Gamma Delta Tocotrienol Alpha Beta Gamma Delta Tocofersolan
K	Naphthoquinone Phylloquinone (K₁) Menaquinones (K₂) Menadione (K₃)‡ Menadiol (K₄)

Water soluble

Combinations

Multivitamins

^#WHO-EM
^‡Withdrawn from market
Clinical trials:
- ^†Phase III
- ^§Never to phase III

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