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Pteridine

From Wikipedia, the free encyclopedia
Aromatic compound made of fused pyrimidine and pyrazine rings
Pteridine
Skeletal formula of pteridine
Skeletal formula of pteridine
Pteridine molecule
C=black, H=white, N=blue
Pteridine molecule
C=black, H=white, N=blue
Names
Preferred IUPAC name
Pteridine[1]
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H ☒N
    Key: CPNGPNLZQNNVQM-UHFFFAOYSA-N ☒N
  • InChI=1/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H
    Key: CPNGPNLZQNNVQM-UHFFFAOYAU
  • C1=CN=C2C(=N1)C=NC=N2
Properties
C6H4N4
Molar mass132.126 g·mol−1
Melting point139.5 °C (283.1 °F; 412.6 K)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Apteridine 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 ofheterocyclic compounds containing a wide variety of substituents on this parent structure.Pterins andflavins are classes of substituted pteridines that have diverse biological roles.[2]

Synthesis of pteridine from4,5-diaminopyrimidine andglyoxal

See also

[edit]

References

[edit]
  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.
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