Dopachrome

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Dopachrome
Dopachrome.svg
Names
IUPAC name
5,6-Dioxo-2,3,5,6-tetrahydro-1H-indole-2-carboxylic acid
Identifiers
3D model (JSmol)
ChemSpider
MeSH dopachrome
  • InChI=1S/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h2-3,6,10H,1H2,(H,13,14)
    Key: VJNCICVKUHKIIV-UHFFFAOYSA-N
  • InChI=1/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h2-3,6,10H,1H2,(H,13,14)
    Key: VJNCICVKUHKIIV-UHFFFAOYAH
  • C1C(NC2=CC(=O)C(=O)C=C21)C(=O)O
Properties
C9H7NO4
Molar mass 193.158 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dopachrome is a cyclization product of L-DOPA and is an intermediate in the biosynthesis of melanin.[1] It may tautomerise to form DHICA.

See also[]

References[]

  1. ^ Pawelek JM (March 1991). "After dopachrome?". Pigment Cell Res. 4 (2): 53–62. doi:10.1111/j.1600-0749.1991.tb00315.x. PMID 1946209.
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