Cas no 143553-09-7 (D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI))
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) Chemical and Physical Properties
Names and Identifiers
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- D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI)
- D-Glucosamine-1-13C hydrochloride
- (4ξ)-2-amino-2-deoxy-D-(1-13C)-xylo-hexopyranose hydrochloride
- 143553-09-7
- DTXSID40746490
- (3R,4R,5S,6R)-3-amino-6-(hydroxymethyl)(213C)oxane-2,4,5-triol;hydrochloride
- 2-Amino-2-deoxy-D-(1-~13~C)glucopyranose--hydrogen chloride (1/1)
- D-Glucosamine-1-13C hydrochloride, 99 atom % 13C
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- Inchi: 1S/C6H13NO5.ClH/c7-3-5(10)4(9)2(1-8)12-6(3)11;/h2-6,8-11H,1,7H2;1H/t2-,3-,4-,5-,6?;/m1./s1/i6+1;
- InChI Key: QKPLRMLTKYXDST-GVSDTCGFSA-N
- SMILES: Cl.O1[13CH]([C@@H]([C@H]([C@@H]([C@H]1CO)O)O)N)O
Computed Properties
- Exact Mass: 215.056
- Monoisotopic Mass: 215.056
- Isotope Atom Count: 1
- Hydrogen Bond Donor Count: 6
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 155
- Covalently-Bonded Unit Count: 2
- 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: nothing
- Topological Polar Surface Area: 116?2
Experimental Properties
- Color/Form: Not determined
- Density: 1.563
- Boiling Point: 449.9°Cat760mmHg
- Flash Point: 225.9°C
- PSA: 116.17000
- LogP: -1.75270
- Solubility: Not determined
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 488739-100MG |
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) |
143553-09-7 | 100mg |
¥10229.19 | 2023-12-05 |
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) Related Literature
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
Additional information on D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI)
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI): A Comprehensive Overview
D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI), with the CAS number 143553-09-7, is a specialized compound that has garnered significant attention in the fields of biochemistry and molecular biology. This compound is a derivative of glucose, a fundamental carbohydrate that plays a pivotal role in energy metabolism. The modifications introduced in this compound—specifically the incorporation of 13C and 15N isotopes—make it highly valuable for advanced research applications.
The structure of D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) is characterized by its unique isotopic labeling. The 13C at position 1 and the amino group (NH) at position 2, which is further labeled with 15N, provide researchers with precise tools for studying metabolic pathways and enzyme kinetics. This labeling allows for non-invasive tracking of glucose metabolism in living systems using techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.
Recent advancements in isotopic labeling techniques have enhanced the utility of this compound in various research domains. For instance, studies have employed this compound to investigate glycolysis pathways in cancer cells, providing insights into how these cells exploit glucose metabolism for rapid growth. Additionally, its use in tracing carbon fluxes in metabolic networks has contributed to a deeper understanding of energy distribution in cellular systems.
The synthesis of D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) involves a multi-step process that ensures high purity and stability. Researchers have optimized synthetic protocols to minimize side reactions and maximize yield, making this compound more accessible for large-scale studies. Furthermore, the hydrochloride salt form ensures solubility in aqueous solutions, facilitating its use in various experimental setups.
In terms of applications, this compound has found extensive use in both basic research and applied sciences. In pharmacology, it serves as a tracer for studying drug metabolism and bioavailability. In the field of nutrition, it aids in assessing carbohydrate utilization efficiency under different dietary conditions. Moreover, its application in biotechnology has been pivotal in developing novel therapeutic strategies targeting metabolic disorders.
Recent studies have highlighted the potential of D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) in personalized medicine. By enabling precise monitoring of metabolic responses to specific treatments, this compound could pave the way for tailored therapies that address individual patient needs more effectively.
In conclusion, D-Glucose-1-13C,2-(amino-15N)-2-deoxy-, hydrochloride (9CI) is a versatile tool that continues to advance our understanding of glucose metabolism and its implications across diverse scientific disciplines. As research progresses, its role in unlocking new therapeutic avenues and improving diagnostic methods is expected to grow significantly.
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