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L-Proline-N-Boc-[15N]

General Information
Catalog: BLP-009517
Molecular Formula: C10H17[15N]O4
Molecular Weight: 216.24
Chemical Structure
L-Proline-N-Boc-[15N]
Description L-Proline-N-Boc-[15N] is a 15N Fmoc-Proline. L-Proline-N-Boc-[15N] can be used in synthesis of 15N labelled amino acid derivatives and peptides. The Boc protecting group can be easily removed by simple operations.
Synonyms Boc-Pro-OH-15N; Boc-L-Proline-15N
Related CAS 15761-39-4 (unlabelled)
InChI InChI=1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1/i11+1
InChI Key ZQEBQGAAWMOMAI-PFGINBISSA-N
Purity 98% by CP; 96% atom 15N
Appearance White Solid

L-Proline-N-Boc-[15N] is an isotopically labeled amino acid derivative used in various research and industrial applications. Here are some key applications of L-Proline-N-Boc-[15N]:

Stable Isotope Labeling: In protein structure studies, L-Proline-N-Boc-[15N] is used as a stable isotope tracer to label specific proline residues. By incorporating this labeled amino acid into proteins, researchers can perform NMR spectroscopy to determine the structural and dynamic properties of proteins at atomic resolution. This helps in understanding protein folding, conformational changes, and interactions with other molecules.

Metabolic Flux Analysis: L-Proline-N-Boc-[15N] is also employed in metabolic flux analysis to investigate proline metabolism pathways in cells. By tracing the labeled nitrogen atom in metabolic networks, scientists can quantify the flow of metabolites and assess the regulation of proline synthesis and degradation. This information is crucial for studying metabolic disorders and developing strategies for metabolic engineering.

Drug Development: In pharmaceutical research, L-Proline-N-Boc-[15N] can be used as a building block in the synthesis of labeled proline-containing compounds. These compounds are valuable in pharmacokinetic studies where the distribution and metabolism of drugs are tracked using isotopic labeling. This aids in understanding drug absorption, bioavailability, and excretion profiles, contributing to the development of more effective therapeutics.

Enzymatic Mechanism Studies: Researchers utilize L-Proline-N-Boc-[15N] in enzymatic studies to explore the mechanisms of proline-utilizing enzymes. By incorporating this labeled compound into enzymatic reactions, scientists can investigate enzyme-substrate interactions and catalytic mechanisms through isotopic labeling experiments. This knowledge assists in elucidating enzyme function and potentially designing enzyme inhibitors for therapeutic applications.

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