Idose

Idose^[1]
Names
	IUPAC name Idose
	Systematic IUPAC name (3S,4R,5R,6R)-6-(Hydroxymethyl)oxane-2,3,4,5-tetrol
Identifiers
CAS Number	2152-76-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	389853 ;
PubChem CID	441034;
UNII	2YL114VI04 ;
	InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4-,5+,6?/m1/s1 Key: WQZGKKKJIJFFOK-YIDFTEPTSA-N ; InChI=1/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4-,5+,6?/m1/s1 Key: WQZGKKKJIJFFOK-YIDFTEPTBS;
	SMILES O[C@@H]1[C@@H](O)[C@H](OC(O)[C@H]1O)CO;
Properties
Chemical formula	C6H12O6
Molar mass	180.156 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

Idose is a hexose, a six carbon monosaccharide. It has an aldehyde group and is an aldose. It is not found in nature, but its uronic acid, iduronic acid, is important. It is a component of dermatan sulfate and heparan sulfate, which are glycosaminoglycans. The first and third hydroxyls point the opposite way from the second and fourth. It is made by aldol condensation of D- and L-glyceraldehyde. L-Idose is a C-5 epimer of D-glucose.

References

This article about an organic compound is a stub. You can help Wikipedia by expanding it.