Indican

Indican

Names
IUPAC name 1H-Indol-3-yl β-D-glucopyranoside
Systematic IUPAC name (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-[(1H-indol-3-yl)oxy]oxane-3,4,5-triol
Identifiers
CAS Number	487-60-5 Y
3D model (JSmol)	Interactive image
ChemSpider	390239 N
ECHA InfoCard	100.126.244
PubChem CID	441564
UNII	N187WK1Y1J Y
CompTox Dashboard (EPA)	DTXSID10903997
InChI InChI=1S/C14H17NO6/c16-6-10-11(17)12(18)13(19)14(21-10)20-9-5-15-8-4-2-1-3-7(8)9/h1-5,10-19H,6H2/t10-,11-,12+,13-,14-/m1/s1 N Key: XVARCVCWNFACQC-RKQHYHRCSA-N N InChI=1/C14H17NO6/c16-6-10-11(17)12(18)13(19)14(21-10)20-9-5-15-8-4-2-1-3-7(8)9/h1-5,10-19H,6H2/t10-,11-,12+,13-,14-/m1/s1 Key: XVARCVCWNFACQC-RKQHYHRCBQ
SMILES C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O
Properties
Chemical formula	C14H17NO6
Molar mass	295.291 g·mol−1
Melting point	178 to 180 °C (352 to 356 °F; 451 to 453 K) (decomposes)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Indican is a colourless organic compound, soluble in water, naturally occurring in Indigofera plants. It is a precursor of indigo dye.^[1]

Chemical reactions

Indican is a glycoside. Common and significant reactions involving indican are as follows:

• The hydrolysis of indican yields β-D-glucose and indoxyl.
• The reaction of indoxyl (indican) with a mild oxidizing agent, such as atmospheric oxygen, yields blue indigo dye.

Medical significance

Biosynthesis

A reaction, similar to that used to produce indigo dye, is seen in the normal population,^[2] who excrete small amounts of the chemical in their urine. Normal urine reacting to hydrogen peroxide does at times produce a bluish tinge. Tryptophan is first converted to indole (which is excreted in faeces), then to indican by bacteria in the gut. Indican, being water-soluble, is then excreted through the urine. Following absorption from the gut, indole is converted to 3-hydroxy indole (indoxyl or indican) in the liver, where it is again then conjugated with sulfuric acid or glucuronic acid through normal xenobiotic metabolism pathways. It is then transported to the kidneys for excretion.^[3][4]

The enzyme "indoxyl esterase" has been found in humans and is involved in another pathway of chemical reactions involving indoxyl.^[5]

Pathology

Individuals affected by blue diaper syndrome exhibit a defect in tryptophan metabolism. Tryptophan is first converted to indole, then to indican by bacteria in the gut. Indican is then excreted into the urine and from there into the diaper where, upon exposure to air, it is oxidised by atmospheric oxygen to indigo blue dye.

Indican interferes with many commercial procedures for measuring total bilirubin^[6] which can be a problem for renal failure patients whose blood indican levels are raised. It can cause gastrointestinal symptoms in patients whose protein absorption is reduced, as in Hartnup's disease, allowing for greater bacterial decomposition of the tryptophan to indole and its conversion to indican.

References

This page was last edited on 9 December 2023, at 23:49