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Robinose

From Wikipedia, the free encyclopedia

Robinose
Names
IUPAC name
6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-galactopyranose
Other names
Robinobiose
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6-,7+,8-,9+,10+,11+,12+/m0/s1
    Key: OVVGHDNPYGTYIT-PEPLWKDOSA-N
  • InChI=1/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6-,7+,8-,9+,10+,11+,12+/m0/s1
    Key: OVVGHDNPYGTYIT-PEPLWKDOBI
  • O(C[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)[C@@H]2O[C@H]([C@H](O)[C@@H](O)[C@H]2O)C
Properties
C12H22O10
Molar mass 326.298 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Robinose is a disaccharide composed of 6″-O-α-rhamnopyranosyl-β-galactopyranoside. The sugar can be found in Acalypha hispida.[1]

Robinin is a kaempferol-3-O-robinoside-7-O-rhamnoside.

References

  1. ^ Reiersen, Bergitte; Kiremire, Bernard T; Byamukama, Robert; Andersen, Øyvind M (2003). "Anthocyanins acylated with gallic acid from chenille plant, Acalypha hispida". Phytochemistry. 64 (4): 867–71. doi:10.1016/S0031-9422(03)00494-1. PMID 14559283.


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This page was last edited on 7 July 2015, at 18:29
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