Pteridine

Pteridine
C=black, H=white, N=blue	C=black, H=white, N=blue
Names
	Preferred IUPAC name Pteridine
Identifiers
CAS Number	91-18-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:27601 ;
ChemSpider	1014 ;
KEGG	C07581 ;
PubChem CID	1043;
UNII	6EZF26XQ81 ;
CompTox Dashboard (EPA)	DTXSID60238347 ;
	InChI InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H Key: CPNGPNLZQNNVQM-UHFFFAOYSA-N ; InChI=1/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H Key: CPNGPNLZQNNVQM-UHFFFAOYAU;
	SMILES C1=CN=C2C(=N1)C=NC=N2;
Properties
Chemical formula	C6H4N4
Molar mass	132.126 g·mol−1
Melting point	139.5 °C (283.1 °F; 412.6 K)
	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

A pteridine is a bicyclic heterocyclic system with two nitrogen atoms at positions 1 and 4 in ring A, and two nitrogen atoms at positions 1 and 3 in ring B. Pteridines constitute a large group of heterocyclic compounds containing a wide variety of substituents on this parent structure. Pterins and flavins are classes of substituted pteridines that have diverse biological roles.^[2]

Synthesis of pteridine from 4,5-diaminopyrimidine and glyoxal

References

^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 212. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
^ Kritsky, M. S; Telegina, T. A; Vechtomova, Y. L; Kolesnikov, M. P; Lyudnikova, T. A; Golub, O. A (2010). "Excited flavin and pterin coenzyme molecules in evolution". Biochemistry. Biokhimiia. 75 (10): 1200–16. doi:10.1134/s0006297910100020. PMID 21166638. S2CID 19455034.1200-16&rft.date=2010&rft_id=https://api.semanticscholar.org/CorpusID:19455034#id-name=S2CID&rft_id=info:pmid/21166638&rft_id=info:doi/10.1134/s0006297910100020&rft.aulast=Kritsky&rft.aufirst=M. S&rft.au=Telegina, T. A&rft.au=Vechtomova, Y. L&rft.au=Kolesnikov, M. P&rft.au=Lyudnikova, T. A&rft.au=Golub, O. A&rfr_id=info:sid/en.wikipedia.org:Pteridine" class="Z3988">

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[1] International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 212. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.

[2] Kritsky, M. S; Telegina, T. A; Vechtomova, Y. L; Kolesnikov, M. P; Lyudnikova, T. A; Golub, O. A (2010). "Excited flavin and pterin coenzyme molecules in evolution". Biochemistry. Biokhimiia. 75 (10): 1200–16. doi:10.1134/s0006297910100020. PMID 21166638. S2CID 19455034.1200-16&rft.date=2010&rft_id=https://api.semanticscholar.org/CorpusID:19455034#id-name=S2CID&rft_id=info:pmid/21166638&rft_id=info:doi/10.1134/s0006297910100020&rft.aulast=Kritsky&rft.aufirst=M. S&rft.au=Telegina, T. A&rft.au=Vechtomova, Y. L&rft.au=Kolesnikov, M. P&rft.au=Lyudnikova, T. A&rft.au=Golub, O. A&rfr_id=info:sid/en.wikipedia.org:Pteridine" class="Z3988">

[2]

[1]

Pteridine

See also

References