Cas no 105931-74-6 (D-Glucose-2-13C)

D-Glucose-2-13C is a stable isotope-labeled form of glucose, where the carbon-2 position is enriched with the 13C isotope. This compound is widely used in metabolic research, tracer studies, and NMR spectroscopy due to its ability to provide precise tracking of glucose metabolism pathways. The 13C label allows for accurate detection and quantification in complex biological systems, making it valuable for investigating glycolysis, gluconeogenesis, and other biochemical processes. Its high isotopic purity and chemical stability ensure reliable experimental results. D-Glucose-2-13C is particularly useful in studies requiring site-specific isotopic labeling to elucidate metabolic fluxes and enzyme mechanisms.
D-Glucose-2-13C structure
D-Glucose-2-13C structure
Product Name:D-Glucose-2-13C
CAS No:105931-74-6
MF:C6H12O6
MW:181.148537635803
CID:126920
PubChem ID:329760198
Update Time:2025-06-11

D-Glucose-2-13C Chemical and Physical Properties

Names and Identifiers

    • D-Glucopyranose-2-13C(9CI)
    • D-Glucose-2-13C
    • α-D-(2-13C)glucopyranose
    • Labeled Glucose
    • dextrose-2-13c
    • D-[2-13C]GLUCOSE
    • D-GLUCOSE (2-13C, 99%)
    • D-GLUCOSE-2-13C, 99 ATOM % 13C
    • D-Glucose-2-13C, S & P tested, 99 atom % 13C
    • J-001503
    • HY-B0389S13
    • 105931-74-6
    • AKOS015915810
    • D-Glucose-13C-3
    • (3R,4S,5S,6R)-6-(hydroxymethyl)(313C)oxane-2,3,4,5-tetrol
    • DTXSID20484449
    • D-Glucose-2-(13-C)
    • CS-0376117
    • (3R,4S,5R,6R)-6-(HYDROXYMETHYL)(3-(1)(3)C)OXANE-2,3,4,5-TETROL
    • MDL: MFCD00037546
    • Inchi: 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1/i5+1
    • InChI Key: WQZGKKKJIJFFOK-UKLRSMCWSA-N
    • SMILES: O1C([13C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O)O

Computed Properties

  • Exact Mass: 181.06674293g/mol
  • Monoisotopic Mass: 181.06674293g/mol
  • Isotope Atom Count: 1
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 151
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: -2.6
  • Topological Polar Surface Area: 110?2

Experimental Properties

  • Color/Form: Not determined
  • Density: 1.732
  • Melting Point: 150-152?°C (lit.)
  • Refractive Index: 1.635
  • PSA: 110.38000
  • LogP: -3.22140
  • Optical Activity: [α]25/D +52.0, c =?2 in H2O (trace NH4OH)
  • Solubility: Not determined

D-Glucose-2-13C Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:1
  • Safety Term:WGK Germany 3

D-Glucose-2-13C Pricemore >>

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D-Glucose-2-13C Related Literature

Additional information on D-Glucose-2-13C

Research Brief on 105931-74-6 and D-Glucose-2-13C: Advances in Chemical Biology and Pharmaceutical Applications

The chemical compound 105931-74-6 and the isotopically labeled glucose derivative D-Glucose-2-13C have garnered significant attention in recent research within the chemical biology and pharmaceutical sectors. These compounds play pivotal roles in metabolic studies, drug development, and diagnostic applications. This research brief synthesizes the latest findings and advancements related to these key substances, providing insights into their applications and implications for future research.

105931-74-6, a compound with specific pharmacological properties, has been investigated for its potential in modulating metabolic pathways. Recent studies highlight its role in targeting enzymes involved in glycolysis and oxidative phosphorylation, making it a candidate for therapeutic interventions in metabolic disorders. Concurrently, D-Glucose-2-13C, a stable isotope-labeled glucose, is extensively utilized in metabolic flux analysis (MFA) to trace carbon flow in biological systems. Its application in cancer research, particularly in understanding the Warburg effect, has provided novel insights into tumor metabolism.

In a 2023 study published in the Journal of Chemical Biology, researchers employed D-Glucose-2-13C to elucidate the metabolic reprogramming in cancer cells. The study demonstrated that the incorporation of 13C-labeled glucose into metabolic intermediates could be quantified using advanced mass spectrometry techniques, offering a precise method to map metabolic networks. This approach has significant implications for developing targeted therapies that disrupt cancer cell metabolism.

Another groundbreaking research effort focused on 105931-74-6 explored its interaction with mitochondrial enzymes. Findings revealed that the compound exhibits inhibitory effects on specific dehydrogenases, thereby altering cellular energy production. These results, published in the European Journal of Medicinal Chemistry, suggest potential applications in treating diseases characterized by mitochondrial dysfunction, such as neurodegenerative disorders and diabetes.

The synergy between 105931-74-6 and D-Glucose-2-13C is also being investigated in preclinical models. For instance, a recent collaborative study between academic and industry researchers utilized both compounds to study metabolic adaptations in drug-resistant bacterial strains. The integration of isotopic tracing with pharmacological inhibition provided a comprehensive understanding of bacterial metabolism under stress conditions, paving the way for novel antibiotic development.

Looking ahead, the continued exploration of 105931-74-6 and D-Glucose-2-13C holds promise for advancing both basic and applied research. Future directions may include the development of more potent derivatives of 105931-74-6 with enhanced selectivity and the application of D-Glucose-2-13C in clinical diagnostics. As these compounds become more integral to research and therapeutic strategies, their impact on chemical biology and pharmaceutical sciences is expected to grow exponentially.

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