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
CAS Number	12698-55-4;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:16214;
ChemSpider	21864805 (6Z,10E,14E);
KEGG	C00110;
MeSH	Dolichol+monophosphate
PubChem CID	24892715 (6Z,10E,14E);
	InChI 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;
	SMILES CC(CCOP(O)(O)=O)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C;
Properties
Chemical formula	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). Infobox references

Dolichol monophosphate is a phosphate ester of dolichol. It is important in biosynthesis of glycoproteins, occurring in several mammalians' organs,^[1] especially the liver.^[2]^[3]

References

↑ Hughes, R. Colin (2014). Membrane Glycoproteins: A Review of Structure and Function (ebook). Elsevier Science. pp. 218–227. ISBN 9781483163963. Retrieved 12 August 2026.
↑ 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.
↑ 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.

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