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L-Tyrosine-[phenol-18O]

General Information
Catalog: BLP-009552
Molecular Formula: C9H11NO2[18O]
Molecular Weight: 183.19
Chemical Structure
L-Tyrosine-[phenol-18O]
Description L-Tyrosine-[phenol-18O], a 18O labelled analogue of L-Tyrosine. L-Tyrosine is biologically converted from L-phenylalanine and in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine.
Related CAS 60-18-4 (unlabelled)
InChI InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1/i5D2,11+2
InChI Key OUYCCCASQSFEME-FFIYMRMASA-N
Purity 98% by CP; 90% atom 18O
Appearance White Solid

L-Tyrosine-[phenol-18O], a labeled amino acid with diverse scientific and industrial uses, finds application in a multitude of fields. Below are the key applications of L-Tyrosine-[phenol-18O]:

Metabolic Tracing: Embedded in metabolic tracing studies, L-Tyrosine-[phenol-18O] plays a pivotal role in tracking and quantifying metabolic pathways. By introducing this labeled amino acid into cellular systems, researchers can meticulously monitor its metabolic trajectory. This method enables an intricate analysis of metabolic fluxes and the intricate mapping of biochemical pathways, shedding light on the intricate dance of cellular metabolism.

Proteomics Research: Delving into the realm of proteomics, L-Tyrosine-[phenol-18O] emerges as a critical tool for investigating protein synthesis, degradation, and turnover in cells. Through the incorporation of this isotope-labeled tyrosine into newly formed proteins, scientists can scrutinize protein dynamics using mass spectrometry. This technique is indispensable for unraveling the complexities of protein function and cellular responses across diverse environments, unveiling the dynamic nature of cellular proteins.

Biomedical Research: Within the realm of biomedical exploration, L-Tyrosine-[phenol-18O] serves as a key player in unraveling the mysteries of enzyme functions and signaling pathways reliant on tyrosine residues. This labeled amino acid aids in the examination of tyrosine phosphorylation, a crucial post-translational modification critical for orchestrating various cellular processes. By leveraging this application, researchers gain valuable insights into the molecular mechanisms underpinning health and disease, illuminating the intricate interplay within cellular signaling networks.

Drug Metabolism Studies: Pioneering drug metabolism studies, L-Tyrosine-[phenol-18O] emerges as a powerful tool for dissecting drug metabolism and pharmacokinetics. Through the labeling of drug molecules or their derivatives with this isotope, researchers can meticulously track the metabolic pathways and biotransformation of drugs within the body. This crucial information plays a pivotal role in optimizing drug design and enhancing therapeutic efficacy, offering a glimpse into the intricate journey of drugs as they navigate the intricate landscape of human metabolism.

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