3,4-Dihydroxymandelic acid
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| Names | |
|---|---|
| IUPAC name
2-(3,4-dihydroxyphenyl)-2-hydroxyacetic acid | |
| Identifiers | |
775-01-9  | |
| ChEBI | CHEBI:27637  |
| ChemSpider | 77371 |
| 6633 | |
| Jmol interactive 3D | Image |
| KEGG | C05580 |
| MeSH | 3,4-dihydroxymandelic+acid |
| PubChem | 85782 |
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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). | |
| verify (what is ?) | |
| 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
- ↑ 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 0-443-06911-5.
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