Isoalloxazine

Isoalloxazine
Names
	IUPAC name 1H-benzo[g]pteridine-2,4-dione
	Other names 1,2,3,4-Tetrahydrobenzopteridine-2,4-dione; Benzo(g)pteridine-2,4(1H,3H)-dione
Identifiers
CAS Number	490-59-5;
3D model (JSmol)	Interactive image;
Beilstein Reference	85819
ChEBI	CHEBI:37325;
ChEMBL	ChEMBL68500;
ChemSpider	4522915;
ECHA InfoCard	100.007.014
EC Number	207-714-3;
IUPHAR/BPS	456;
PubChem CID	5372720;
UNII	880W3VF9YW;
CompTox Dashboard (EPA)	DTXSID50197656 ;
	InChI InChI=1S/C10H6N4O2/c15-9-7-8(13-10(16)14-9)12-6-4-2-1-3-5(6)11-7/h1-4H,(H2,12,13,14,15,16) Key: HAUGRYOERYOXHX-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)N=C3C(=N2)NC(=O)NC3=O;
Properties
Chemical formula	C10H6N4O2
Molar mass	214.184 g·mol−1
Appearance	Red solid
Melting point	200 °C (392 °F; 473 K)[1]
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Isoalloxazine is the structural foundation of flavins such as riboflavin (vitamin B2) and is a heterocyclic compound.[2] It has a tricyclic structure which means it has three interconnected rings of atoms and is a tautomer of alloxazine.[1] The structure is formed by primary-secondary aromatic o-diamines and they are a high-melting crystalline substance.[1] The R-group is used to attach various flavin groups It has a similar structure to pteridines which has two interconnected rings.[1] Isoalloxazine was first obtained in 1934[1] by Richard Kuhn an Austrian-German biochemist and lab mates.

Isoalloxazine Structure

Isoalloxazine ring

Isoalloxazine rings can exist in different redox and ionization states depending on the chemistry of FMN and FAD associated with it.[3] Using the redox-active isoalloxazine system, FAD and FMN are able to do one and two electron transfer reactions and also be coupled with proton transfers [4]

Ionization and redox states of the isoalloxazine ring

References

Berezovskii, VM; Eremenko, TV (1963). "Chemistry of Alloxazines and Isoalloxazines". Russian Chemical Reviews. 32 (6): 290–307. doi:10.1070/RC1963v032n06ABEH001343. Retrieved November 23, 2022.
"isoalloxazine". Farlex Partner Medical Dictionary. 2012. Retrieved November 25, 2022.
Luliano, James N. (2019). "Vibrational spectroscopy of flavoproteins". New Approaches for Flavin Catalysis. Methods in Enzymology. Vol. 620 (volume 620 ed.). Methods in Enzymology: Elsevier Inc. pp. 189–214. doi:10.1016/bs.mie.2019.03.011. ISBN 9780128168295. ISSN 0076-6879. PMID 31072487. S2CID 146800749.
Aleksandrov, Alexey (2019). "A Molecular Mechanics Model for Flavins". Journal of Computational Chemistry. 40 (32): 2834–2842. doi:10.1002/jcc.26061. PMID 31471978. S2CID 201730443.

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[Berezovskii1963-1] Berezovskii, VM; Eremenko, TV (1963). "Chemistry of Alloxazines and Isoalloxazines". Russian Chemical Reviews. 32 (6): 290–307. doi:10.1070/RC1963v032n06ABEH001343. Retrieved November 23, 2022.

[2] "isoalloxazine". Farlex Partner Medical Dictionary. 2012. Retrieved November 25, 2022.

[3] Luliano, James N. (2019). "Vibrational spectroscopy of flavoproteins". New Approaches for Flavin Catalysis. Methods in Enzymology. Vol. 620 (volume 620 ed.). Methods in Enzymology: Elsevier Inc. pp. 189–214. doi:10.1016/bs.mie.2019.03.011. ISBN 9780128168295. ISSN 0076-6879. PMID 31072487. S2CID 146800749.

[4] Aleksandrov, Alexey (2019). "A Molecular Mechanics Model for Flavins". Journal of Computational Chemistry. 40 (32): 2834–2842. doi:10.1002/jcc.26061. PMID 31471978. S2CID 201730443.