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Revision as of 19:51, 21 September 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'ChemSpiderID_Ref', 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEBI_Ref') per [[WP:CHEMVALID|Chem/Drugbox validation← Previous edit Revision as of 17:06, 12 February 2012 edit undoThe chemistds (talk | contribs)Extended confirmed users5,761 edits added PubchemID, CSID, (Std)InChI & (Std)InChIKeyNext edit →
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| Section1 = {{Chembox Identifiers | Section1 = {{Chembox Identifiers
| CASNo = 2152-76-3 | CASNo = 2152-76-3
| PubChem = | PubChem = 441034
| ChemSpiderID = 389853
| SMILES = O1(O)<br>(O)(O)C(CO)O1 | SMILES = O1(O)(OC(O)1O)CO
| 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
| InChIKey = WQZGKKKJIJFFOK-YIDFTEPTBS
| StdInChI = 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
| StdInChIKey = WQZGKKKJIJFFOK-YIDFTEPTSA-N
}} }}
| Section2 = {{Chembox Properties | Section2 = {{Chembox Properties

Revision as of 17:06, 12 February 2012

For the so-called digital drug, see I-Doser.
Idose
Names
IUPAC names 6-(hydroxymethyl)oxane-
2,3,4,5-tetrol
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
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/s1Key: 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/s1Key: WQZGKKKJIJFFOK-YIDFTEPTBS
SMILES
  • O1(O)(OC(O)1O)CO
Properties
Chemical formula C6H12O6
Molar mass 180.16
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

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

  1. ' Merck Index, 11th Edition, 4818
Types of carbohydrates
General
Geometry
Monosaccharides
Dioses
Trioses
Tetroses
Pentoses
Hexoses
Heptoses
Above 7
Multiple
Disaccharides
Trisaccharides
Tetrasaccharides
Other
oligosaccharides
Polysaccharides
Category: