Homogentisate

Homogentisic acid

Names
IUPAC name (2,5-Dihydroxyphenyl)acetic acid
Other names Melanic acid
Identifiers
CAS Number	451-13-8 Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:44747 Y
ChemSpider	759 Y
DrugBank	DB08327 Y
ECHA InfoCard	100.006.540
KEGG	C00544 Y
MeSH	Homogentisic+acid
PubChem	780
InChI InChI=1S/C8H8O4/c9-6-1-2-7(10)5(3-6)4-8(11)12/h1-3,9-10H,4H2,(H,11,12) Y Key: IGMNYECMUMZDDF-UHFFFAOYSA-N Y InChI=1/C8H8O4/c9-6-1-2-7(10)5(3-6)4-8(11)12/h1-3,9-10H,4H2,(H,11,12) Key: IGMNYECMUMZDDF-UHFFFAOYAK
SMILES O=C(O)Cc1cc(O)ccc1O
Properties
Chemical formula	C8H8O4
Molar mass	168.15 g·mol−1
Melting point	150 to 152 °C (302 to 306 °F; 423 to 425 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

Homogentisic acid (2,5-dihydroxyphenylacetic acid) is a phenolic acid found in Arbutus unedo (strawberry-tree) honey. It is also present in the bacterial plant pathogen Xanthomonas campestris pv. phaseoli as well as in the yeast Yarrowia lipolytica where it is associated with the production of brown pigments.

It is less commonly known as melanic acid, the name chosen by William Prout.

Accumulation of excess homogentisic acid and its oxide, named alkapton, is a result of the failure of the enzyme homogentisic acid 1,2-dioxygenase (typically due to a mutation) in the degradative pathway of tyrosine, consequently associated with alkaptonuria.

It is an intermediate in the catabolism of aromatic amino acids such as phenylalanine and tyrosine.