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CHEBI:90327 - 2-nitrophenyl N-acetyl-α-D-glucosaminide
| Formula | C14H18N2O8 |
| Net Charge | 0 |
| Average Mass | 342.304 |
| Monoisotopic Mass | 342.10632 |
| SMILES | CC(=O)N[C@H]1[C@@H](Oc2ccccc2[N+](=O)[O-])O[C@H](CO)[C@@H](O)[C@@H]1O |
| InChI | InChI=1S/C14H18N2O8/c1-7(18)15-11-13(20)12(19)10(6-17)24-14(11)23-9-5-3-2-4-8(9)16(21)22/h2-5,10-14,17,19-20H,6H2,1H3,(H,15,18)/t10-,11-,12-,13-,14+/m1/s1 |
| InChIKey | PXMQUEGJJUADKD-KSTCHIGDSA-N |
| Roles Classification |
|---|
| Biological Roles: | mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). 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) |
| 2-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90327) has functional parent 2-nitrophenol (CHEBI:16260) |
| 2-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90327) has role chromogenic compound (CHEBI:75050) |
| 2-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90327) is a C-nitro compound (CHEBI:35716) |
| 2-nitrophenyl N-acetyl-α-D-glucosaminide (CHEBI:90327) is a N-acetyl-α-D-glucosaminide (CHEBI:27425) |
| IUPAC Name |
|---|
| 2-nitrophenyl 2-acetamido-2-deoxy-α-D-glucopyranoside |
| Synonyms | Source |
|---|---|
| 2'-Nitrophenyl-2-acetamido-2-deoxy-alpha-D-glucopyranoside | ChemIDplus |
| o-nitrophenyl N-acetyl-α-D-glucosaminide | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1663751 | Reaxys |
| CAS:10139-01-2 | ChemIDplus |