Chemistry:3,4-Dihydroxymandelic acid

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3,4-Dihydroxymandelic acid
3,4-Dihydroxymandelic acid.svg
Names
Preferred IUPAC name
(3,4-Dihydroxyphenyl)(hydroxy)acetic acid
Other names
2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
MeSH 3,4-dihydroxymandelic+acid
UNII
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).
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Infobox references

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. ↑ Ley JP; Engelhart K; Bernhardt J; Bertram HJ (October 2002). "3,4-Dihydroxymandelic acid, a noradrenalin metabolite with powerful antioxidative potential". J. Agric. Food Chem. 50 (21): 5897–902. doi:10.1021/jf025667e. PMID 12358456. 
  2. ↑ 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. 

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| name = Neurotransmitter metabolism intermediates
| title = Neurotransmitter metabolic intermediates
| state = autocollapse|
| listclass = hlist

| group1 = catecholamines
  | list1 = {{Navbox|child

  | group1 = Anabolism
(tyrosine→epinephrine)
  | list1 =

  | group2 = Catabolism/
metabolites

| list2 =

dopamine:
norepinephrine:
epinephrine:
}} 

| group3 = tryptophan→serotonin
| list3 =
anabolism:
catabolism:
| group4 = serotonin→melatonin
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