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DL-Proline-[1-13C]

General Information
Catalog: BLP-008133
CAS: 212258-93-0
Molecular Formula: C4[13C]H9NO2
Molecular Weight: 116.13
Chemical Structure
DL-Proline-[1-13C]
Description DL-Proline-[1-13C] is a labelled DL-Proline. Proline is the only proteinogenic amino acid with a secondary amine. It can be used as an asymmetric catalyst in proline organocatalysis reactions.
Synonyms DL-Proline 1-13C
Related CAS 609-36-9 (unlabelled)
Canonical SMILES C1CC(NC1)C(=O)O
InChI InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/i5+1
InChI Key ONIBWKKTOPOVIA-HOSYLAQJSA-N
Purity 98% by HPLC; 99% atom 13C
Storage Store at -20°C

DL-Proline-[1-13C], a stable isotopically labeled compound, finds diverse applications in research. Here are the key applications of DL-Proline-[1-13C]:

Metabolic Flux Analysis: Utilizing DL-Proline-[1-13C] for metabolic flux analysis enables the tracing of proline metabolism pathways. By introducing this labeled compound into cells or organisms, researchers can track the carbon flow through various biochemical routes. This approach aids in unraveling the intricacies of metabolic dynamics and pinpointing pivotal regulatory nodes within metabolism.

Protein Structure Studies: Leveraging DL-Proline-[1-13C] in nuclear magnetic resonance (NMR) spectroscopy facilitates the investigation of protein structures. The 13C labeling generates distinctive signals that can be detected and scrutinized, offering researchers insights into protein folding, stability, and interactions. This application plays a critical role in advancing structural biology and informing drug design strategies.

Biomarker Discovery: In the realm of clinical research, DL-Proline-[1-13C] serves as a valuable tool for identifying and quantifying metabolic biomarkers linked to various diseases. By analyzing the labeled metabolites present in biological samples, scientists can uncover diagnostic markers indicative of underlying disease conditions or responses to treatments. This capability fuels the development of non-invasive diagnostic assays and personalized therapeutic approaches.

Kinetic Studies: Employing DL-Proline-[1-13C] for kinetic studies allows for the exploration of reaction kinetics within biochemical pathways. By monitoring the incorporation and turnover of the labeled proline, researchers can measure the rates of reactions and kinetics of enzymes involved in proline metabolism. This data is instrumental in enhancing our understanding of enzyme functions and in designing enzyme modulators for therapeutic interventions.

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