Cas no 105931-74-6 (D-Glucose-2-13C)
D-Glucose-2-13C Chemical and Physical Properties
Names and Identifiers
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- 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
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- 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 >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | G595008-25mg |
D-Glucose-2-13C |
105931-74-6 | 25mg |
$ 138.00 | 2023-09-07 | ||
| TRC | G595008-250mg |
D-Glucose-2-13C |
105931-74-6 | 250mg |
$ 856.00 | 2023-09-07 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D132193-1g |
D-Glucose-2-13C |
105931-74-6 | 99 atom % 13C | 1g |
¥4686.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D132193-250mg |
D-Glucose-2-13C |
105931-74-6 | 99 atom % 13C | 250mg |
¥1462.90 | 2023-09-03 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 310794-250MG |
D-Glucose-2-13C |
105931-74-6 | 250mg |
¥3928.3 | 2023-12-08 | ||
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 310794-1G |
D-Glucose-2-13C |
105931-74-6 | 1g |
¥11332.14 | 2023-12-08 | ||
| Omicron Biochemicals | GLC-020-0.25g |
D-[2-13C]glucose |
105931-74-6 | 0.25g |
$150 | 2025-08-06 | ||
| Omicron Biochemicals | GLC-020-0.50g |
D-[2-13C]glucose |
105931-74-6 | 0.50g |
$235 | 2025-08-06 | ||
| Omicron Biochemicals | GLC-020-1.0g |
D-[2-13C]glucose |
105931-74-6 | 1.0g |
$380 | 2025-08-06 | ||
| Omicron Biochemicals | GLC-020-1g |
D-[2-13C]glucose |
105931-74-6 | 1g |
$305 | 2023-09-21 |
D-Glucose-2-13C Related Literature
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Muge Niu,Yucui Hou,Weize Wu,Shuhang Ren,Ru Yang Phys. Chem. Chem. Phys. 2018 20 17942
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Zhichao Tan,Gai Miao,Chang Liu,Hu Luo,Liwei Bao,Lingzhao Kong,Yuhan Sun RSC Adv. 2016 6 62747
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Ana Cecilia Ho-Palma,Floriana Rotondo,María del Mar Romero,Serena Memmolo,Xavier Remesar,José Antonio Fernández-López,Marià Alemany Anal. Methods 2016 8 7873
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Sangeeta Mahala,Senthil M. Arumugam,Sandeep Kumar,Bhawana Devi,Sasikumar Elumalai Nanoscale Adv. 2023 5 2470
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5. Bacterial sterol surrogates. Biosynthesis of the side-chain of bacteriohopanetetrol and of a carbocyclic pseudopentose from 13C-labelled glucose in Zymomonas mobilisMichel Rohmer,Bertrand Sutter,Hermann Sahm J. Chem. Soc. Chem. Commun. 1989 1471
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.