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Lumiflavin

From Wikipedia, the free encyclopedia
Lumiflavin
Names
Preferred IUPAC name
7,8,10-Trimethylbenzo[g]pteridine-2,4(3H,10H)-dione
Other names
Lumilactoflavin
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
ECHA InfoCard100.012.841Edit this at Wikidata
UNII
  • InChI=1S/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19) checkY
    Key: KPDQZGKJTJRBGU-UHFFFAOYSA-N checkY
  • InChI=1/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19)
    Key: KPDQZGKJTJRBGU-UHFFFAOYAD
  • O=C2/N=C\1/N(c3cc(c(cc3/N=C/1C(=O)N2)C)C)C
Properties
C13H12N4O2
Molar mass256.265 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Lumiflavin is atoxic product ofphotolysis ofvitamin B2.[1]

References

[edit]
  1. ^Rodríguez-Otero, Jesús; Martínez-Núñez, Emilio; Peña-Gallego, Angeles; Vázquez, Saulo A (2002). "The Role of Aromaticity in the Planarity of Lumiflavin".The Journal of Organic Chemistry.67 (18):6347–6352.doi:10.1021/jo011159c.PMID 12201752.
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