Lumiflavin

Lumiflavin
Names
	Preferred IUPAC name 7,8,10-Trimethylbenzo[g]pteridine-2,4(3H,10H)-dione
	Other names Lumilactoflavin
Identifiers
CAS Number	1088-56-8 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:43661 ;
ChemSpider	59571 ;
DrugBank	DB04726 ;
ECHA InfoCard	100.012.841
PubChem CID	66184;
UNII	4M2669414M ;
CompTox Dashboard (EPA)	DTXSID10148745 ;
	InChI 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) Key: KPDQZGKJTJRBGU-UHFFFAOYSA-N ; 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;
	SMILES O=C2/N=C\1/N(c3cc(c(cc3/N=C/1C(=O)N2)C)C)C;
Properties
Chemical formula	C13H12N4O2
Molar mass	256.265 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Lumiflavin is a toxic product of photolysis of vitamin B₂.^[1]

References

^ 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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[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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