5-Oxo-L-proline-d5 is a deuterated form of 5-oxo-L-proline, which is a derivative of proline, an amino acid. This compound is characterized by the presence of a five-membered lactam ring, which includes a carbonyl group (C=O) adjacent to the nitrogen atom of the proline structure. The "d5" designation indicates that five hydrogen atoms in the molecule have been replaced with deuterium, a stable isotope of hydrogen, which is often used in NMR spectroscopy and other analytical techniques to trace molecular interactions and dynamics. The presence of deuterium enhances the compound's stability and can improve the resolution of spectroscopic data. 5-Oxo-L-proline itself is involved in various biochemical processes, including the synthesis of other amino acids and metabolic pathways. Its deuterated form is particularly useful in research settings, where it can serve as a tracer or standard in studies involving metabolic pathways or protein interactions. As with many chemical substances, handling should be done with care, following appropriate safety protocols.

5-Oxo-L-proline-d5

1086136-22-2: 5-Oxo-L-proline-d5 is a deuterated form of 5-oxo-L-proline, which is a derivative of proline, an amino acid. This compound is characterized by the presence of a five-membered lactam ring, which includes a carbonyl group (C=O) adjacent to the nitrogen atom of the proline structure. The "d5" designation indicates that five hydrogen atoms in the molecule have been replaced with deuterium, a stable isotope of hydrogen, which is often used in NMR spectroscopy and other analytical techniques to trace molecular interactions and dynamics. The presence of deuterium enhances the compound's stability and can improve the resolution of spectroscopic data. 5-Oxo-L-proline itself is involved in various biochemical processes, including the synthesis of other amino acids and metabolic pathways. Its deuterated form is particularly useful in research settings, where it can serve as a tracer or standard in studies involving metabolic pathways or protein interactions. As with many chemical substances, handling should be done with care, following appropriate safety protocols.

L-2-Pyrrolidinone-3,3,4,4,5-d5-5-carboxylic Acid

<p>Applications 5-Oxo-L-proline-d5 is a labelled cyclized derivative of L-Glutamic Acid (G596960). The pyroglutamate core has potential application for synthesis of novel anti-bacterials.<br>References Mischo A. et al.: ChemBioChem., 13, 1421 (2012); Angelov P. et al.: Org. Biomol. Chem.: 10, 3472 (2012);<br></p>

CAS 1086136-22-2

5-Oxo-L-proline-d5

L-2-Pyrrolidinone-3,3,4,4,5-d5-5-carboxylic Acid

Ref: 3U-D3715

5-Oxo-L-proline-d5

Ref: TR-O858977