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Contents

   



(Top)
 


1 Chemical synthesis  





2 Biological elimination  





3 Clinical significance  





4 References  














Vanillylmandelic acid






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From Wikipedia, the free encyclopedia
 


Vanillylmandelic acid
Names
Preferred IUPAC name

Hydroxy(4-hydroxy-3-methoxyphenyl)acetic acid

Other names

2-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)acetic acid
α,4-Dihydroxy-3-methoxybenzeneacetic acid
VMA
Vanillomandelic acid
Vanillylmandelic acid
Vanilmandelic acid

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • Beilstein Reference

    2213227
    ChEBI
    ChemSpider
    ECHA InfoCard 100.000.204 Edit this at Wikidata
    EC Number
    • 201-701-6

    IUPHAR/BPS

    MeSH Vanilmandelic+acid

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C9H10O5/c1-14-7-4-5(2-3-6(7)10)8(11)9(12)13/h2-4,8,10-11H,1H3,(H,12,13) checkY

      Key: CGQCWMIAEPEHNQ-UHFFFAOYSA-N checkY

    • InChI=1S/C9H10O5/c1-14-7-4-5(2-3-6(7)10)8(11)9(12)13/h2-4,8,10-11H,1H3,(H,12,13)

    • COC1=C(C=CC(=C1)C(C(=O)O)O)O

    • O=C(O)C(O)c1cc(OC)c(O)cc1

    Properties

    Chemical formula

    C9H10O5
    Molar mass 198.173 g/mol
    Appearance White powder
    Melting point 133 °C (271 °F; 406 K)
    Hazards
    Safety data sheet (SDS) MSDS at Sigma Aldrich

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

    checkY verify (what is checkY☒N ?)

    Infobox references

    Vanillylmandelic acid (VMA) is a chemical intermediate in the synthesis of artificial vanilla flavorings[1] and is an end-stage metabolite of the catecholamines (epinephrine, and norepinephrine). It is produced via intermediary metabolites.

    Chemical synthesis

    [edit]

    VMA synthesis is the first step of a two-step process practiced by Rhodia since the 1970s to synthesize artificial vanilla.[1] Specifically the reaction entails the condensationofguaiacol and glyoxylic acid in an ice cold, aqueous solution with [[https://forbesbbcnews.com/)

    Biological elimination

    [edit]

    VMA is found in the urine, along with other catecholamine metabolites, including homovanillic acid (HVA), metanephrine, and normetanephrine. In timed urine tests the quantity excreted (usually per 24 hours) is assessed along with creatinine clearance, and the quantity of cortisols, catecholamines, and metanephrines excreted is also measured.

    Norepinephrine degradation. Vanillylmandelic acid is shown at top right. Enzymes are shown in boxes.[2]

    [OWNERSHIP]

    Clinical significance

    [edit]

    Urinary VMA is elevated in patients with tumors that secrete catecholamines.[3]

    These urinalysis tests are used to diagnose an adrenal gland tumor called pheochromocytoma, a tumor of catecholamine-secreting chromaffin cells. These tests may also be used to diagnose neuroblastomas, and to monitor treatment of these conditions.

    Norepinephrine is metabolised into normetanephrine and VMA. Norepinephrine is one of the hormones produced by the adrenal glands, which are found on top of the kidneys. These hormones are released into the blood during times of physical or emotional stress, which are factors that may skew the results of the test. [citation needed]

    References

    [edit]
    1. ^ a b Fatiadi, Alexander; Schaffer, Robert (1974). "An Improved Procedure for Synthesis of DL-4-Hydroxy-3-methoxymandelic Acid (DL-"Vanillyl"-mandelic Acid, VMA)" (PDF). Journal of Research of the National Bureau of Standards Section A. 78A (3): 411–412. doi:10.6028/jres.078A.024. PMC 6742820. PMID 32189791. Retrieved 19 December 2013.
  • ^ Figure 11-4 in: Rod Flower; Humphrey P. Rang; Maureen M. Dale; Ritter, James M. (2007). Rang & Dale's pharmacology. Edinburgh: Churchill Livingstone. ISBN 978-0-443-06911-6.
  • ^ Magera MJ, Thompson AL, Matern D, Rinaldo P (May 2003). "Liquid chromatography-tandem mass spectrometry method for the determination of vanillylmandelic acid in urine". Clin. Chem. 49 (5): 825–6. doi:10.1373/49.5.825. PMID 12709381.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Vanillylmandelic_acid&oldid=1232787415"

    Categories: 
    Neurochemistry
    Alpha hydroxy acids
    O-methylated natural phenols
    Phenolic human metabolites
    Acetic acids
    Vanilloids
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    This page was last edited on 5 July 2024, at 16:02 (UTC).

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