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| Formula | C13H14N2OS |
| Net Charge | 0 |
| Average Mass | 246.335 |
| Monoisotopic Mass | 246.08268 |
| SMILES | N[C@@H](CS)C(=O)Nc1ccc2ccccc2c1 |
| InChI | InChI=1S/C13H14N2OS/c14-12(8-17)13(16)15-11-6-5-9-3-1-2-4-10(9)7-11/h1-7,12,17H,8,14H2,(H,15,16)/t12-/m0/s1 |
| InChIKey | NCMHLYITDACZJV-LBPRGKRZSA-N |
| Roles Classification |
|---|
| Biological Role: | human xenobiotic metabolite Any human metabolite produced by metabolism of a xenobiotic compound in humans. |
| 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) |
| L-cysteine 2-naphthylamide (CHEBI:90426) has role chromogenic compound (CHEBI:75050) |
| L-cysteine 2-naphthylamide (CHEBI:90426) has role human xenobiotic metabolite (CHEBI:76967) |
| L-cysteine 2-naphthylamide (CHEBI:90426) is a N-(2-naphthyl)carboxamide (CHEBI:88330) |
| L-cysteine 2-naphthylamide (CHEBI:90426) is a L-cysteine derivative (CHEBI:83824) |
| L-cysteine 2-naphthylamide (CHEBI:90426) is a amino acid amide (CHEBI:22475) |
| IUPAC Name |
|---|
| N-naphthalen-2-yl-L-cysteinamide |
| Synonyms | Source |
|---|---|
| Cysteine-beta-naphthylamide | ChemIDplus |
| L-cysteine β-naphthylamide | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:3137048 | Reaxys |
| CAS:65322-97-6 | ChemIDplus |
| Citations |
|---|