CHEBI:90253 - 4-nitrophenyl α-L-fucoside

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 4-nitrophenyl α-L-fucoside
ChEBI ASCII Name 4-nitrophenyl alpha-L-fucoside
Definition An α-L-fucoside that is α-L-fucopyranose 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 C12H15NO7
Net Charge 0
Average Mass 285.250
Monoisotopic Mass 285.085
InChI InChI=1S/C12H15NO7/c1-6-9(14)10(15)11(16)12(19-6)20-8-4-2-7(3-5-8)13(17)18/h2-6,9-12,14-16H,1H3/t6-,9+,10+,11-,12-/m0/s1
SMILES O1[C@H]([C@H]([C@H]([C@@H]([C@@H]1OC=2C=CC(=CC2)[N+]([O-])=O)O)O)O)C
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via alpha-L-fucoside )
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 α-L-fucoside (CHEBI:90253) has functional parent 4-nitrophenol (CHEBI:16836)
4-nitrophenyl α-L-fucoside (CHEBI:90253) has role chromogenic compound (CHEBI:75050)
4-nitrophenyl α-L-fucoside (CHEBI:90253) is a α-L-fucoside (CHEBI:28349)
4-nitrophenyl α-L-fucoside (CHEBI:90253) is a C-nitro compound (CHEBI:35716)
4-nitrophenyl α-L-fucopyranoside
Synonyms Sources
4-nitrophenyl 6-deoxy-α-L-galactopyranoside IUPAC
4-Nitrophenylfucoside ChemIDplus
p-Nitrophenyl 6-deoxy-alpha-L-galactopyranoside ChemIDplus
p-nitrophenyl α-L-fucoside ChEBI
Registry Numbers Types Sources
10231-84-2 CAS Registry Number ChemIDplus
89535 Reaxys Registry Number Reaxys
Last Modified
06 November 2015