Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-013252 |
Molecular Formula: C5[13C]H14ClNO5 |
Molecular Weight: 216.63 |
Chemical Structure |
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Description | A labelled analogue of D-Glucosamine Hydrochloride. D-Glucosamine HCl is an HCl salt glucosasmine preparation. It has been used as a standard to quantify and express chitin content as glucosamine equivalents. It is used to stimulate cells with glucose in the presence of glucosamine. |
Synonyms | 2-Amino-2-deoxy-D-glucose-2-13C Hydrochloride; D-Glucosamine-2-13C hydrochloride; 2-amino-2-deoxy-D-[2-13C]glucose hydrochloride; D-[2-13C]glucosamine hydrochloride; 2-Deoxy-2-amino-D-glucose-2-13C hydrochloride; D-(+)-Glucosamine-2-13C hydrochloride; Chitosamine-2-13C hydrochloride |
Related CAS | 66-84-2 (unlabelled) 3416-24-8 (unlabelled free base) |
Melting Point | >180°C (dec.) |
Solubility | Soluble in Water |
Appearance | White Solid |
2-amino-2-deoxy-D-glucose-[2-13C] hydrochloride is a stable isotope-labeled glucose analog used for a variety of applications in biochemical and preclinical research. Here are some key applications:
Metabolic Flux Analysis: This compound is used in metabolic flux analysis to track glucose utilization and metabolism within cells. By incorporating the labeled glucose into metabolic pathways, researchers can quantify fluxes through glycolysis and other pathways. This helps in understanding cellular energy production, metabolic reprogramming in diseases, and the effects of pharmacological interventions.
Cancer Research: 2-amino-2-deoxy-D-glucose-[2-13C] hydrochloride is utilized in cancer research to study tumor metabolism. Cancer cells often exhibit altered glucose metabolism, known as the Warburg effect, which can be monitored using this labeled glucose analog. This information can assist in identifying abnormal metabolic pathways and potential therapeutic targets in oncology.
Neuroimaging: In neuroimaging studies, this compound is used in conjunction with techniques such as Magnetic Resonance Spectroscopy (MRS) to visualize and measure brain metabolism. It allows researchers to investigate glucose uptake and utilization in various brain regions under different physiological and pathological conditions. This is particularly valuable in studying conditions like Alzheimer's disease and other neurological disorders.
Pharmacokinetics: 2-amino-2-deoxy-D-glucose-[2-13C] hydrochloride can be used to study the pharmacokinetics and bioavailability of drugs that influence glucose metabolism. By tracking the labeled glucose in vivo, researchers can evaluate how drugs affect glucose uptake, distribution, and utilization. This can provide insights into drug efficacy and safety, as well as metabolic side effects.
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