Article · Wikipedia archive · Last revised Jun 17, 2026

Apiose

Apiose is a branched-chain sugar found as residues in galacturonans-type pectins; that occurs in parsley and many other plants. Apiose is a component of cell wall polysaccharides.

Last revised
Jun 17, 2026
Read time
≈ 1 min
Length
169 w
Citations
2
Source
Apiose
Chemical structure of apiose
Chemical structure of apiose source ↗
Names
IUPAC name
3-C-(Hydroxymethyl)-glycero-tetrose1
Systematic IUPAC name
2,3,4-Trihydroxy-3-(hydroxymethyl)butanal
Other names
  • D-Apiose
    3-C-(Hydroxymethyl)-D-glycerotetrose
  • Apio-β-D-furanose
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 sugar found as residues in galacturonans-type pectins; that occurs in parsley and many other plants. Apiose is a component of cell wall polysaccharides.2

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

Flavone apiosyltransferase uses UDP-apiose and 5,7,4'-trihydroxyflavone 7-O-β-D-glucoside to produce UDP, 5,7,4'-trihydroxyflavone (apigenin), and 7-O-β-D-apiosyl-(1->2)-β-apiitol-glucoside.

References

References

  1. https://old.iupac.org/publications/pac/1996/pdf/6810x1919.pdf
  2. Pičmanová, Martina; Møller, Birger Lindberg (2016). "Apiose: One of nature's witty games". Glycobiology. 26 (5): 430–442. doi:10.1093/glycob/cww012. PMID 26848180.
External links

The dictionary definition of apiose at Wiktionary