3,4-Dihydroxymandelic acid

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Dcirovic (talk | contribs) at 04:15, 14 May 2016 (corected authors list (CS1 maint)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

3,4-Dihydroxymandelic acid
Names
IUPAC name
2-(3,4-dihydroxyphenyl)-2-hydroxyacetic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.011.154 Edit this at Wikidata
KEGG
MeSH 3,4-dihydroxymandelic+acid
  • InChI=1S/C8H8O5/c9-5-2-1-4(3-6(5)10)7(11)8(12)13/h1-3,7,9-11H,(H,12,13) checkY
    Key: RGHMISIYKIHAJW-UHFFFAOYSA-N checkY
  • InChI=1/C8H8O5/c9-5-2-1-4(3-6(5)10)7(11)8(12)13/h1-3,7,9-11H,(H,12,13)
    Key: RGHMISIYKIHAJW-UHFFFAOYAB
  • O=C(O)C(O)c1cc(O)c(O)cc1
Properties
C8H8O5
Molar mass 184.14612
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

3,4-Dihydroxymandelic acid (DHMA, DOMA) is a metabolite of norepinephrine.[1]

Norepinephrine degradation. 3,4-Dihydroxymandelic acid is shown at right. Enzymes are shown in boxes.[2]

References

  1. ^ "3,4-Dihydroxymandelic acid, a noradrenalin metabolite with powerful antioxidative potential". J. Agric. Food Chem. 50 (21): 5897–902. October 2002. doi:10.1021/jf025667e. PMID 12358456. {{cite journal}}: Cite uses deprecated parameter |authors= (help)
  2. ^ Figure 11-4 in: Rang & Dale's pharmacology. Edinburgh: Churchill Livingstone. 2007. ISBN 0-443-06911-5. {{cite book}}: Cite uses deprecated parameter |authors= (help)


Stub icon

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=3,4-Dihydroxymandelic_acid&oldid=720167760"