Xanthopterin

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Xanthopterin
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Names
IUPAC name
Xanthopterin
Identifiers
119-44-8 N
ChemSpider 8091 YesY
Jmol 3D model Interactive image
PubChem 8397
UNII V66551EU1R YesY
  • InChI=1S/C6H5N5O2/c7-6-10-4-3(5(13)11-6)9-2(12)1-8-4/h1H,(H,9,12)(H3,7,8,10,11,13) YesY
    Key: VURKRJGMSKJIQX-UHFFFAOYSA-N YesY
  • InChI=1S/C6H5N5O2/c7-6-10-4-3(5(13)11-6)9-2(12)1-8-4/h1H,(H,9,12)(H3,7,8,10,11,13)
  • O=C1/N=C(\NC=2/N=C\C(=O)NC1=2)N
Properties
C6H5N5O2
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Xanthopterin is a yellow, crystalline solid[1] that occurs mainly in the wings of butterflies and in the urine of mammals.[1] Small microorganisms convert it into folic acid.[2] It is the end product of a non-conjugated pteridine compound[3] and inhibits the growth of lymphocytes produced by concanavalin.[3] High levels of the chemical were found in patients with liver disease and hemolysis, the latter increasing levels by 35%.[4][5]

The Oriental hornet uses xanthopterin as a light-harvesting molecule to transform light into electrical energy, which explains why the insects are more active when light intensity is greater. It remains an active and important area of scientific research (Plotkin et al., Naturwissenschaften (2010) 97:1067–1076).[6]

References

  1. 1.0 1.1 http://cancerweb.ncl.ac.uk/cgi-bin/omd?xanthopterin
  2. http://medical.merriam-webster.com/medical/xanthopterin
  3. 3.0 3.1 http://content.karger.com/ProdukteDB/produkte.asp?Doi=46271
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