3,4-Dihydroxymandelic acid

3,4-Dihydroxymandelic acid
Names
	Preferred IUPAC name (3,4-Dihydroxyphenyl)hydroxyacetic acid
	Other names 2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid
Identifiers
CAS Number	775-01-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:27637 ;
ChemSpider	77371 ;
ECHA InfoCard	100.011.154
IUPHAR/BPS	6633;
KEGG	C05580 ;
MeSH	3,4-dihydroxymandelic+acid
PubChem CID	85782;
	InChI 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) Key: RGHMISIYKIHAJW-UHFFFAOYSA-N ; 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;
	SMILES O=C(O)C(O)c1cc(O)c(O)cc1;
Properties
Chemical formula	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

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.

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