Aspartylglucosamine[1] is a derivative of aspartic acid.

Aspartylglucosamine
Names
IUPAC name
(2S)-4-[[(2R,3R,4R,5S,6R)-3-Acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-2-amino-4-oxobutanoic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
MeSH N-acetylglucosaminylasparagine
UNII
  • InChI=1S/C12H21N3O8/c1-4(17)14-8-10(20)9(19)6(3-16)23-11(8)15-7(18)2-5(13)12(21)22/h5-6,8-11,16,19-20H,2-3,13H2,1H3,(H,14,17)(H,15,18)(H,21,22)/t5-,6+,8+,9+,10+,11+/m0/s1 checkY
    Key: YTTRPBWEMMPYSW-HRRFRDKFSA-N checkY
  • InChI=1/C12H21N3O8/c1-4(17)14-8-10(20)9(19)6(3-16)23-11(8)15-7(18)2-5(13)12(21)22/h5-6,8-11,16,19-20H,2-3,13H2,1H3,(H,14,17)(H,15,18)(H,21,22)/t5-,6+,8+,9+,10+,11+/m0/s1
    Key: YTTRPBWEMMPYSW-HRRFRDKFBT
  • CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1NC(=O)C[C@@H](C(=O)O)N)CO)O)O
Properties
C12H21N3O8
Molar mass 335.31 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Levels are elevated in aspartylglucosaminuria.[2]

References

edit
  1. ^ PubChem. "N-aspartylglucosamine". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-01-13.
  2. ^ "Aspartylglucosaminuria i". ISMRD — The International Advocate for Glycoprotein Storage Diseases.