
TE-L-Tyrosine (FET-precursor) | CAS 478037-15-9
| Catalog Number | A16-0226 |
| Category | Other Cell Fluorescent Probes |
| Molecular Formula | C41H43NO6S |
| Molecular Weight | 677.86 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
TE-L-Tyrosine is a precursor for O-(2-[18F]fluoroethyl)-L-tyrosine (FET), which is a widely used F18-labeled amino acid tracer for positron emission tomography and computed tomography (PET/CT).
Chemical Information
Application
Chemical Information
| Synonyms | (S)-tert-Butyl 3-(4-(2-(tosyloxy)ethoxy)phenyl)-2-(tritylamino)propanoate; O-(2-tosyloxyethyl)-N-trityl-l-tyrosine tert-butylester |
| IUPAC Name | tert-butyl (2S)-3-[4-[2-(4-methylphenyl)sulfonyloxyethoxy]phenyl]-2-(tritylamino)propanoate |
| SMILES | CC1=CC=C(C=C1)S(=O)(=O)OCCOC2=CC=C(C=C2)CC(C(=O)OC(C)(C)C)NC(C3=CC=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5 |
| InChI | InChI=1S/C41H43NO6S/c1-31-20-26-37(27-21-31)49(44,45)47-29-28-46-36-24-22-32(23-25-36)30-38(39(43)48-40(2,3)4)42-41(33-14-8-5-9-15-33,34-16-10-6-11-17-34)35-18-12-7-13-19-35/h5-27,38,42H,28-30H2,1-4H3/t38-/m0/s1 |
| InChIKey | KSGPTMKBCVMBBB-LHEWISCISA-N |
Application
TE-L-Tyrosine (FET-precursor) is a tyrosine-based building block designed for incorporation into fluorescent enzyme technology (FET) and related fluorescence-tagging workflows. As a precursor, it is commonly used by chemical biology and assay development teams to construct fluorescently informative conjugates where tyrosine chemistry supports downstream labeling and signal readout in bioanalytical formats. Researchers leverage this reagent to prepare tyrosine-containing constructs that integrate into fluorescence-based detection strategies, including imaging and plate-based readouts, where consistent precursor handling is important for reproducible reagent performance.
1. Fluorescent Enzyme Technology Labeling
TE-L-Tyrosine (FET-precursor) is used by bioconjugation and diagnostics R&D groups to build FET-enabled labeling reagents that translate biochemical recognition or processing into fluorescence output. In these workflows, the tyrosine precursor serves as a key input for preparing fluorescently functional conjugates used in assay development, including reagent screening and method optimization in fluorescence-based analytical pipelines. Teams developing fluorescence-tagged biomolecules, including enzyme-associated or substrate-like constructs, often select tyrosine-precursor chemistry to maintain workflow consistency across batches.
2. Fluorescence-Based Bioassay Reagent Development
TE-L-Tyrosine (FET-precursor) supports the development of fluorescence readout reagents for bioassays where tyrosine-containing constructs are incorporated into assay components that generate measurable signal in microplate and benchtop formats. Assay developers in chemical biology and molecular diagnostics research use the precursor to assemble standardized reagent sets for evaluating reaction conditions, timing, and labeling performance in fluorescence assays. The reagent's role as a precursor helps streamline the preparation of assay-ready fluorescent conjugate intermediates used in iterative assay prototyping.
3. Molecular Imaging Probe Construction
TE-L-Tyrosine (FET-precursor) is applied in fluorescence probe construction for molecular imaging studies that require tyrosine-derived precursor incorporation into fluorescently informative labeling constructs. Imaging groups use the reagent to prepare probe intermediates that integrate into fluorescence-based visualization workflows, including localization studies where probe performance depends on reproducible precursor-to-conjugate preparation. By using a tyrosine precursor platform, researchers can align probe construction with established fluorescence-tagging strategies used for cellular and biomolecular imaging experiments.
4. Fluorescent Conjugate Engineering
TE-L-Tyrosine (FET-precursor) is used in conjugate engineering programs that require tyrosine-containing components to be integrated into fluorescently functional materials and biomolecule conjugates. Materials and chemical biology teams incorporate the precursor into multi-component labeling schemes to produce fluorescent conjugates for downstream use in labeling workflows, including reagent libraries for method development. This application is especially common in groups that prioritize modular precursor inputs to support consistent conjugate assembly and characterization during fluorescence reagent development.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry