Cas no 39063-89-3 (2,3,3,4,4,5,5-d7-L-Proline)

2,3,3,4,4,5,5-d7-L-Proline structure
2,3,3,4,4,5,5-d7-L-Proline structure
Product Name:2,3,3,4,4,5,5-d7-L-Proline
CAS No:39063-89-3
MF:C5H9NO2
MW:122.1735932827
CID:4673694
PubChem ID:102351655
Update Time:2025-04-23

2,3,3,4,4,5,5-d7-L-Proline Chemical and Physical Properties

Names and Identifiers

    • 2,3,3,4,4,5,5-d7-L-Proline
    • L-Proline (D7, 97-98%)
    • CHEBI:192088
    • (2S)-2,3,3,4,4,5,5-heptadeuteriopyrrolidine-2-carboxylic acid
    • 39063-89-3
    • HY-Y0252S5
    • CS-0376543
    • L-Proline-d7
    • Inchi: 1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1/i1D2,2D2,3D2,4D
    • InChI Key: ONIBWKKTOPOVIA-BFEYZEMLSA-N
    • SMILES: C([C@]1(NC([2H])([2H])C([2H])([2H])C1([2H])[2H])[2H])(=O)O

Computed Properties

  • Exact Mass: 122.107265751g/mol
  • Monoisotopic Mass: 122.107265751g/mol
  • Isotope Atom Count: 7
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 1
  • Complexity: 103
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.5
  • Topological Polar Surface Area: 49.3?2

2,3,3,4,4,5,5-d7-L-Proline Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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2,3,3,4,4,5,5-d7-L-Proline Production Method

Production Method 1

Reaction Conditions
Reference
Investigation of the dynamics of aqueous proline solutions using neutron scattering and molecular dynamics simulations
Malo de Molina, Paula; Alvarez, Fernando; Frick, Bernhard; Wildes, Andrew; Arbe, Arantxa; et al, Physical Chemistry Chemical Physics, 2017, 19(40), 27739-27754

2,3,3,4,4,5,5-d7-L-Proline Raw materials

2,3,3,4,4,5,5-d7-L-Proline Preparation Products

2,3,3,4,4,5,5-d7-L-Proline Related Literature

Additional information on 2,3,3,4,4,5,5-d7-L-Proline

Introduction to L-Proline-d7 (CAS No. 39063-89-3) and Its Applications in Modern Chemical Biology

L-Proline-d7, a deuterated isotope of the common amino acid L-proline, is a compound of significant interest in the field of chemical biology and pharmaceutical research. With the CAS number 39063-89-3, this molecule has garnered attention due to its unique properties and potential applications in various scientific domains. L-Proline-d7 is particularly valued for its use as a labeled biomolecule, enabling researchers to trace metabolic pathways and study protein dynamics with high precision.

The structure of L-Proline-d7 consists of a six-carbon backbone with a hydrogen atom replaced by a deuterium atom at the 4-position, making it a stable isotope suitable for NMR spectroscopy and mass spectrometry studies. This modification enhances the resolution and sensitivity of analytical techniques, allowing for more accurate characterization of complex biological systems. The deuterated form also minimizes interference from endogenous proline in biological samples, providing clearer insights into enzymatic reactions and metabolic processes.

In recent years, the demand for labeled amino acids has surged, particularly in the development of proteomics and metabolomics tools. L-Proline-d7 plays a crucial role in these fields by enabling researchers to track the incorporation of proline into proteins and peptides. This is particularly useful in studying post-translational modifications, such as phosphorylation and glycosylation, which are essential for understanding protein function and regulation. The use of L-Proline-d7 in these studies has led to significant advancements in our understanding of cellular signaling pathways and disease mechanisms.

One of the most compelling applications of L-Proline-d7 is in the field of drug discovery and development. Pharmaceutical companies are increasingly utilizing deuterated compounds to improve drug efficacy and reduce side effects. The incorporation of deuterium atoms into drug molecules can alter their metabolic stability, leading to longer half-lives and improved bioavailability. For instance, studies have shown that deuterated analogs of proline-based drugs exhibit enhanced pharmacokinetic profiles, making them more effective in treating various conditions.

The synthesis of L-Proline-d7 presents unique challenges due to the need for precise isotopic labeling. Advanced chemical synthesis techniques, such as catalytic hydrogenation and isotopic exchange reactions, are employed to achieve high levels of deuterium incorporation while maintaining the structural integrity of the molecule. These methods require careful optimization to ensure that the final product meets the stringent purity standards required for biological applications.

Recent research has also explored the use of L-Proline-d7 in studying enzyme kinetics and substrate inhibition. By monitoring the binding and reaction rates of deuterated proline with various enzymes, scientists can gain insights into the mechanisms underlying enzymatic catalysis. This information is crucial for designing inhibitors with higher specificity and potency, which could lead to novel therapeutic agents.

The versatility of L-Proline-d7 extends beyond its use as a labeled biomolecule. It has found applications in analytical chemistry, where it serves as an internal standard for quantitative analysis. Its stable isotope nature allows for accurate calibration of instruments used in mass spectrometry and NMR spectroscopy, ensuring reliable data interpretation. This has been particularly beneficial in environmental monitoring studies, where trace levels of proline need to be detected in complex matrices.

In conclusion, L-Proline-d7 (CAS No. 39063-89-3) is a highly valuable compound with numerous applications in chemical biology and pharmaceutical research. Its unique properties make it an ideal candidate for studying metabolic pathways, protein dynamics, drug development, and analytical chemistry. As research continues to evolve, the importance of labeled biomolecules like L-Proline-d7 will only grow, driving further advancements in our understanding of biological systems and disease treatment.

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