2-Amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid
97%
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This compound is primarily utilized in biochemical research due to its structural similarity to tryptophan, a crucial amino acid. It is often employed in studies investigating the role of fluorine substitution in biological systems, particularly in enzyme interactions and receptor binding. Its fluorinated indole structure makes it valuable for probing metabolic pathways and designing fluorinated analogs of bioactive molecules. Additionally, it serves as a building block in the synthesis of novel peptides and pharmaceuticals, especially those targeting neurological disorders or cancer, where fluorine incorporation can enhance stability and bioavailability. Its unique properties also make it a candidate for fluorescence labeling in imaging and diagnostic applications.
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