Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Dopachrome

From Wikipedia, the free encyclopedia
Dopachrome
Names
IUPAC name
5,6-Dioxo-2,3,5,6-tetrahydro-1H-indole-2-carboxylic acid
Identifiers
3D model (JSmol)
ChemSpider
MeSHdopachrome
UNII
  • 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 mass193.158 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Dopachrome is a cyclization product ofL-DOPA and is an intermediate in thebiosynthesis ofmelanin.[1] It maytautomerise to formDHICA.

See also

[edit]

References

[edit]
  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.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Dopachrome&oldid=1175853756"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp