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Contents

   



(Top)
 


1 Biosynthesis  





2 References  





3 External links  














Pantoic acid






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From Wikipedia, the free encyclopedia
 

(Redirected from Pantolactone)

Pantoic acid
Names
Preferred IUPAC name

(2R)-2,4-Dihydroxy-3,3-dimethylbutanoic acid

Other names

D-Pantoic acid; D-Pantoate; B(R)-2,4-dihydroxy-3,3-dimethylbutanoic acid

Identifiers

CAS Number

3D model (JSmol)

ChemSpider

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C6H12O4/c1-6(2,3-7)4(8)5(9)10/h4,7-8H,3H2,1-2H3,(H,9,10)/t4-/m0/s1

    Key: OTOIIPJYVQJATP-BYPYZUCNSA-N

  • O=C(O)[C@H](O)C(C)(C)CO

Properties

Chemical formula

C6H12O4
Molar mass 148.158 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Pantoic acid is the alpha hydroxy acid with the formula HOCH2C(CH3)2CH(OH)CO2H. The compound is almost always encountered in a biological context, as an aqueous solution of its conjugate base pantoate HOCH2C(CH3)2CH(OH)CO2-. The amide of pantoic acid with β-alanineispantothenic acid (vitamin B5),[1] a component of coenzyme A.

Biosynthesis

[edit]

Its biosynthesis proceeds from ketoisovaleratebyhydroxymethylation:

(CH3)2CHC(O)CO2 + CH2O → HOCH2(CH3)2CC(O)CO2

This conversion is catalyzed by ketopantoate hydroxymethyltransferase, which gives ketopantoate. Ketopantoate is reduced by ketopantoate reductase to pantoate, using NADH as the hydride source.[2]

The amide derived from pantoic acid and GABA is the pharmaceutical drug hopantenic acid.

References

[edit]
  1. ^ Pantoic acid, Merriam Webster Medical Dictionary
  • ^ Begley, Tadhg P.; Kinsland, Cynthia; Strauss, Erick (2001). "The Biosynthesis of Coenzyme a in Bacteria". Cofactor Biosynthesis. Vitamins & Hormones. Vol. 61. pp. 157–171. doi:10.1016/S0083-6729(01)61005-7. ISBN 9780127098616. PMID 11153265.
  • [edit]


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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Pantoic_acid&oldid=1044549840"

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    This page was last edited on 15 September 2021, at 20:46 (UTC).

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