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

ChEBI IDCHEBI:90253
ChEBI Name4-nitrophenyl α-L-fucoside
Stars
ASCII Name4-nitrophenyl alpha-L-fucoside
DefinitionAn α-L-fucoside that is α-L-fucopyranose in which the anomeric hydroxy hydrogen is replaced by a 4-nitrophenyl group.
Last Modified6 November 2015
SubmitterSteve
DownloadsMolfile
FormulaC12H15NO7
Net Charge0
Average Mass285.252
Monoisotopic Mass285.08485
SMILESC[C@@H]1O[C@@H](Oc2ccc([N+](=O)[O-])cc2)[C@@H](O)[C@H](O)[C@@H]1O
InChIInChI=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
InChIKeyYILIDCGSXCGACV-SQKFTNEHSA-N
Roles Classification
Biological Role:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Application:
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.
ChEBI Ontology
Outgoing Relation(s)
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 C-nitro compound (CHEBI:35716)
4-nitrophenyl α-L-fucoside (CHEBI:90253) is a α-L-fucoside (CHEBI:28349)
IUPAC Name 
4-nitrophenyl α-L-fucopyranoside
Synonyms  Source
p-nitrophenyl α-L-fucosideChEBI
4-NitrophenylfucosideChemIDplus
p-Nitrophenyl 6-deoxy-alpha-L-galactopyranosideChemIDplus
4-nitrophenyl 6-deoxy-α-L-galactopyranosideIUPAC
Registry NumbersSources
Reaxys:89535Reaxys
CAS:10231-84-2ChemIDplus