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Names | |
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Preferred IUPAC name
(3,4-Dihydroxyphenyl)(hydroxy)acetic acid | |
Other names
2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.011.154 |
KEGG | |
MeSH | 3,4-dihydroxymandelic+acid |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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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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3,4-Dihydroxymandelic acid (DHMA, DOMA) is a metabolite of norepinephrine.[1]
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References
[edit]- ^ 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.
- ^ 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.