Apiose

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Apiose
Chemical structure of apiose
Names
IUPAC name
2,3,4-Trihydroxy-3-(hydroxymethyl)butanal
Other names
D-Apiose
3-C-(Hydroxymethyl)-D-glycerotetrose
Apio-β-D-furanosyl
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C5H10O5/c6-1-5(9)2-10-4(8)3(5)7/h3-4,6-9H,1-2H2/t3-,4?,5+/m0/s1 checkY
    Key: ASNHGEVAWNWCRQ-LJJLCWGRSA-N checkY
  • InChI=1/C5H10O5/c6-1-5(9)2-10-4(8)3(5)7/h3-4,6-9H,1-2H2/t3-,4?,5+/m0/s1
    Key: ASNHGEVAWNWCRQ-LJJLCWGRBE
  • O[C@]1(CO)COC(O)[C@@H]1O
Properties
C5H10O5
Molar mass 150.130 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Apiose is a branched-chain

polysaccharides.[1]

Apiose 1-reductase uses D-apiitol and NAD+ to produce apiitol-apiose, NADH, and H+.

5,7,4'-trihydroxyflavone
(apigenin), and 7-O-β-D-apiosyl-(1->2)-β-apiitol-glucoside.

References

External links

The dictionary definition of apiose at Wiktionary

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