Mannose 1-phosphate

Mannose 1-phosphate
Names
IUPAC name
1-O-Phosphono-D-mannopyranose
Systematic IUPAC name
[(3S,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate
Other names
Mannose-1-P; D-mannose-1-phosphate; D-Mannopyranose-1-phosphate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C6H13O9P/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13/h2-10H,1H2,(H2,11,12,13)/t2-,3-,4+,5+,6?/m1/s1 Y
    Key: HXXFSFRBOHSIMQ-QTVWNMPRSA-N Y
  • O=P(O)(OC1O[C@@H]([C@@H](O)[C@H](O)[C@@H]1O)CO)O
Properties
C6H13O9P
Molar mass 260.135 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Mannose 1-phosphate is a molecule involved in glycosylation. Mannose 1-phosphate can be efficiently synthesised using D-mannose or Methyl alpha-D-mannopyranoside as the starting material.[1]

See also

References

  1. ^ Fey, Sven; Elling, Lothar; Kragl, Udo (December 1997). "The cofactor Mg2+—a key switch for effective continuous enzymatic production of GDP-mannose using recombinant GDP-mannose pyrophosphorylase". Carbohydrate Research. 305 (3–4): 475–481. doi:10.1016/S0008-6215(97)10095-7.