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Bulk Quantity N-AcetyI-L-Tryptophan 丨CAS 1218-34-4
Chemical Identifiers
| InChI | InChI=1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)/t12-/m0/s1 |
| InChI Key | DZTHIGRZJZPRDV-LBPRGKRZSA-N |
| Smiles | CC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O |
| EC No. | 214-935-9 |
| MDL No. | MFCD00065976 |
| PubChem CID | 700653 |
Applications
Pharmaceutical Research and Drug Discovery
Modified amino acids are useful research compounds in medicinal chemistry because changes to functional groups can influence molecular interactions and chemical behavior. N-Acetyl-L-Tryptophan may serve as a research material or synthetic intermediate in studies involving tryptophan derivatives and other indole-containing compounds. Its suitability for a particular pharmaceutical research pathway depends on the target structure and validated synthetic approach.
Biochemical and Metabolic Research
Tryptophan is an important amino acid investigated in protein chemistry, metabolism, and molecular interactions. N-Acetyl-L-Tryptophan can support research examining modified amino acids, the influence of N-acetylation on molecular properties, and the behavior of tryptophan derivatives in defined experimental systems. Its application depends on the specific biochemical question and research model.
Organic Synthesis and Indole Chemistry
Analytical Chemistry and Reference Research
Structurally defined amino acid derivatives can be useful in analytical method development and compound characterization. N-Acetyl-L-Tryptophan may be used in suitable analytical workflows to investigate identity, purity, stability, and the behavior of acetylated amino acid derivatives. Applications requiring reference-standard performance should be supported by appropriate characterization and quality documentation.

