| ID | C0194  |
| Compound name | Phenylalanine |
| Stereochemistry | D,L-Phenylalanine |
| Aracyc name | L-Phenylalanine |
| External link |
 http://pmn.plantcyc.org/ARA/NEW-IMAGE?type=COMPOUND&object=PHE
|
| Mass information |
1st experiment : GC-TOF/MS 2nd experiment : LC-Q-TOF/MS (Positive ion mode) |
| Molecular Formula | H11N1O2C9 |
| Canonical SMILES | C(=O)([O-])C([N+])CC1(C=CC=CC=1) |
| Molecular Weight | 165.191 |
| Pathway Information | suberin biosynthesis, benzoate biosynthesis II (CoA-independent, non-beta-oxidative), indole-3-acetyl-amino acid biosynthesis, phenylalanine degradation III, jasmonoyl-amino acid conjugates biosynthesis I, trans-cinnamoyl-CoA biosynthesis, phenylethanol biosynthesis, phenylalanine biosynthesis II, tRNA charging, IAA degradation V, glucosinolate biosynthesis from phenylalanine, phenylpropanoid biosynthesis, initial reactions |
| CAS ID | 63-91-2 |
| Synonym | F; endophenyl; phenylalanine; phe |
| External ID | CHEBI:58095, PUBCHEM:6925665, LIGAND-CPD:C00079 |
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