Aspartylglucosamine

Aspartylglucosamine

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ImageFile=Aspartylglucosamine.pngImageSize=200px
IUPACName=(2"S")-4- [(2"R",3"R",4"R",5"S",6"R")-3-Acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] amino] -2-amino-4-oxobutanoic acid
OtherNames=
Section1=Chembox Identifiers
CASNo=2776-93-4
PubChem=123826
SMILES=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
MeSHName=N-acetylglucosaminylasparagine
Section2=Chembox Properties
Formula=C12H21N3O8
MolarMass=335.31 g/mol
Appearance=
Density=
MeltingPt=
BoilingPt=
Solubility=
Section3=Chembox Hazards
MainHazards=
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Aspartylglucosamine is a derivative of aspartic acid.

Levels are elevated in aspartylglucosaminuria.


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Look at other dictionaries:

  • aspartylglucosamine — as·par·tyl·glu·co·sa·mine (ə spahr″təl gloo kōsґə mēn) N acetylglucosamine in N glycosidic linkage with the amino group of asparagine; it is an intermediate in the degradation of glycoproteins and accumulates… …   Medical dictionary

  • Aspartylglucosaminuria — Infobox Disease Name = PAGENAME Caption = Aspartylglucosamine DiseasesDB = 952 ICD10 = ICD10|E|77|1|e|70 ICD9 = ICDO = OMIM = 208400 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aspartylglucosaminuria (AGU), also called… …   Wikipedia

  • aspartylglucosaminuria — as·par·tyl·glu·co·sa·min·uria (ə spahr″təl gloo″kōs am″in uґre ə) a severe autosomal recessive lysosomal storage disease caused mutations in the AGA gene (locus: 4q32 q33), which encodes… …   Medical dictionary

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