CHEBI:90341 - 4-nitrophenyl N-acetyl-α-D-glucosaminide

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ChEBI Name 4-nitrophenyl N-acetyl-α-D-glucosaminide
ChEBI ASCII Name 4-nitrophenyl N-acetyl-alpha-D-glucosaminide
Definition An N-acetyl-α-D-glucosaminide in which the anomeric hydroxy hydrogen is replaced by a 4-nitrophenyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C14H18N2O8
Net Charge 0
Average Mass 342.302
Monoisotopic Mass 342.10632
InChI InChI=1S/C14H18N2O8/c1-7(18)15-11-13(20)12(19)10(6-17)24-14(11)23-9-4-2-8(3-5-9)16(21)22/h2-5,10-14,17,19-20H,6H2,1H3,(H,15,18)/t10-,11-,12-,13-,14+/m1/s1
SMILES O1[C@@H]([C@H]([C@@H]([C@H]([C@H]1OC=2C=CC(=CC2)[N+]([O-])=O)NC(=O)C)O)O)CO
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via N-acetyl-D-glucosaminide )
(via D-glucosaminide )
Application(s): chromogenic compound
Colourless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into coloured compounds. They are used in biochemical assays and in diagnosis as indicators, particularly in the form of enzyme substrates.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 4-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90341) has functional parent 4-nitrophenol (CHEBI:16836)
4-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90341) has role chromogenic compound (CHEBI:75050)
4-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90341) is a C-nitro compound (CHEBI:35716)
4-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90341) is a N-acetyl-α-D-glucosaminide (CHEBI:27425)
4-nitrophenyl 2-acetamido-2-deoxy-α-D-glucopyranoside
Synonyms Sources
4'-Nitrophenyl-2-acetamido-2-deoxy-alpha-D-glucopyranoside ChemIDplus
4-nitrophenyl 2-acetamido-2-deoxy-α-D-glucoside ChEBI
p-nitrophenyl 2-acetamido-2-deoxy-α-D-glucoside ChEBI
p-nitrophenyl N-acetyl-α-D-glucosaminide ChEBI
Registry Numbers Types Sources
10139-02-3 CAS Registry Number ChemIDplus
1269349 Reaxys Registry Number Reaxys
Last Modified
12 November 2015