Homovanillic acid

Homovanillic acid

Names
Preferred IUPAC name (4-Hydroxy-3-methoxyphenyl)acetic acid
Other names 2-(4-Hydroxy-3-methoxyphenyl)acetic acid; 3-Methoxy-4-hydroxyphenylacetic acid; 4-Hydroxy-3-methoxy-benzeneacetic acid
Identifiers
CAS Number	306-08-1 Y
3D model ( JSmol )	Interactive image
ChEBI	CHEBI:545959 Y
ChEMBL	ChEMBL1562 Y
ChemSpider	1675 Y
ECHA InfoCard	100.005.616
KEGG	C05582 Y
MeSH	Homovanillic+acid
PubChem CID	1738
UNII	X77S6GMS36 Y
CompTox Dashboard (EPA)	DTXSID5059791
InChI InChI=1S/C9H10O4/c1-13-8-4-6(5-9(11)12)2-3-7(8)10/h2-4,10H,5H2,1H3,(H,11,12) Y Key: QRMZSPFSDQBLIX-UHFFFAOYSA-N Y InChI=1/C9H10O4/c1-13-8-4-6(5-9(11)12)2-3-7(8)10/h2-4,10H,5H2,1H3,(H,11,12) Key: QRMZSPFSDQBLIX-UHFFFAOYAZ
SMILES O=C(O)Cc1cc(OC)c(O)cc1
Properties
Chemical formula	C9H10O4
Molar mass	182.175 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Homovanillic acid (HVA) is a major catecholamine metabolite that is produced by a consecutive action of monoamine oxidase and catechol-O-methyltransferase on dopamine.^[1] Homovanillic acid is used as a reagent to detect oxidative enzymes, and is associated with dopamine levels in the brain.

In psychiatry and neuroscience, brain and cerebrospinal fluid levels of HVA are measured as a marker of metabolic stress caused by 2-deoxy-D-glucose.^[2] HVA presence supports a diagnosis of neuroblastoma and malignant pheochromocytoma.

Fasting plasma levels of HVA are known to be higher in females than in males.^[