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Sku CI21831_10_G
Chem Impex
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Product Information

Product Name
5-Fluoro-DL-tryptophan
Brand Name
Chem Impex
Product Number
21831
CAS
154-08-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
9577
IUPAC Name
2-amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid
InChI Key
INPQIVHQSQUEAJ-UHFFFAOYSA-N
SMILES
C1=CC2=C(C=C1F)C(=CN2)CC(C(=O)O)N

Description

5-Fluoro-DL-tryptophan is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a valuable building block in the synthesis of new pharmaceuticals, particularly in the development of drugs targeting neurological disorders.

Biochemical Research: It is used in studies exploring the role of tryptophan derivatives in metabolic pathways, helping researchers understand their impact on human health.

Protein Engineering: The incorporation of 5-Fluoro-DL-tryptophan into proteins can alter their properties, making it useful for creating proteins with enhanced stability or altered functionality.

Neuroscience Studies: This compound is employed in research investigating serotonin pathways, contributing to the understanding of mood disorders and potential treatments.

Analytical Chemistry: It serves as a standard in various analytical techniques, aiding in the quantification of tryptophan levels in biological samples.

References Data Source From Pubchem

γ9δ2 T cells detect mevalonate diphosphate via BTN3A3

Publication Name: Cellular and molecular life sciences : CMLS
Publication Date: 2025-11-14
DOI: 10.1007/s00018-025-05931-2

Bacillus toyonensis BAR1, a yellow-pigment producing endophyte of Berberis aristata DC: a potential source of bioactive and antimicrobial compounds

Publication Name: Folia Microbiologica
Publication Date: 2025-09-05
DOI: 10.1007/s12223-025-01318-9

Reducing experimental time through spin-lattice relaxation enhancement via dissolved oxygen

Publication Name: Journal of Biomolecular NMR
Publication Date: 2025-02-17
DOI: 10.1007/s10858-024-00457-4

Fluorine-19 labeling of the tryptophan residues in the G protein-coupled receptor NK1R using the 5-fluoroindole precursor in Pichia pastoris expression

Publication Name: Journal of Biomolecular NMR
Publication Date: 2024-03-30
DOI: 10.1007/s10858-024-00439-6

Fluorine labelling for in situ 19F NMR in oriented systems

Publication Name: Journal of Biomolecular NMR
Publication Date: 2024-02-26
DOI: 10.1007/s10858-024-00438-7