Dolichol monophosphate

Dolichol monophosphate
Names
Preferred IUPAC name
[3,7,11,15,19-pentamethylicosa-6,10,14,18-tetraenyl] dihydrogen phosphate
Systematic IUPAC name
[(3,7,11,15,19-pentamethylicosa-6,10,14,18-tetraen-1-yl)oxy]phosphonic acid
Other names
Dolichol phosphate
Dolichyl monophosphate
Dolichyl phosphate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
MeSH Dolichol+monophosphate
  • InChI=1S/C25H45O4P/c1-21(2)11-7-12-22(3)13-8-14-23(4)15-9-16-24(5)17-10-18-25(6)19-20-29-30(26,27)28/h11,13,15,17,25H,7-10,12,14,16,18-20H2,1-6H3,(H2,26,27,28)
    Key: GYBNOAFGEKAZTA-UHFFFAOYSA-N
  • CC(CCOP(O)(O)=O)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C
Properties
C25H45O4P
Molar mass 440.605 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Dolichol monophosphate is a phosphate ester of dolichol. It is important in biosynthesis of glycoproteins, occurring in several mammalians' organs, especially the liver.

See also

References

  1. ↑ Hughes, R. Colin (2014). Membrane Glycoproteins: A Review of Structure and Function (ebook). Elsevier Science. pp. 218–227. ISBN 9781483163963. Retrieved 12 August 2026.
  2. ↑ Schechter, Harry; Rodén, Lennart (2014). The Biosynthesis of Animal Glycoproteins, in Metabolic Conjugation and Metabolic Hydrolysis, Volume 3. Academic Press. pp. 1–2, 49–50. ISBN 9781483269467. Retrieved 12 August 2026.
  3. ↑ T. W. Goodwin, ed. (2014). Biochemistry of Lipids: Biochemistry Series One (ebook). Butterworth-Heinemann. pp. 75–82, 86, 92–93. ISBN 9781483269467. Retrieved 12 August 2026.