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-004460 |
Molecular Formula: C17H17D3FN3O3 |
Molecular Weight: 336.38 |
Chemical Structure |
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Description | Pefloxacin-[d3], is the labelled analogue of Pefloxacin. Pefloxacin is a quinolone antibiotic used to treat bacterial infections. |
Synonyms | Pefloxacin D3 |
IUPAC Name | 1-ethyl-6-fluoro-4-oxo-7-[4-(trideuteriomethyl)piperazin-1-yl]quinoline-3-carboxylic acid |
Related CAS | 70458-92-3 (unlabelled) |
Canonical SMILES | CCN1C=C(C(=O)C2=CC(=C(C=C21)N3CCN(CC3)C)F)C(=O)O |
InChI | InChI=1S/C17H20FN3O3/c1-3-20-10-12(17(23)24)16(22)11-8-13(18)15(9-14(11)20)21-6-4-19(2)5-7-21/h8-10H,3-7H2,1-2H3,(H,23,24)/i2D3 |
InChI Key | FHFYDNQZQSQIAI-BMSJAHLVSA-N |
Purity | 95% by CP; 98% atom D |
Pefloxacin-[d3], a deuterated analogue of the antibiotic pefloxacin, is a valuable tool in research for investigating drug metabolism and pharmacokinetics. Here are the key applications of Pefloxacin-[d3]:
Drug Metabolism Studies: Pefloxacin-[d3] plays a pivotal role in drug metabolism investigations, shedding light on the intricate pharmacokinetic properties of pefloxacin. The deuterated compound acts as a guiding beacon, tracing metabolic pathways and unveiling metabolites in biological samples. This critical data is indispensable for fine-tuning dosages and enhancing therapeutic effectiveness.
Mass Spectrometry: With deuterium atoms integrated into its structure, Pefloxacin-[d3] emerges as a standout performer in mass spectrometry analyses, distinguished and detectable with heightened precision. It stands as an internal benchmark for quantifying pefloxacin concentrations in complex biological matrices. This meticulous quantification is paramount for monitoring drug levels in pharmacokinetic evaluations and ensuring adherence to therapeutic protocols.
Pharmacodynamic Research: Delving into the dynamics of drug interactions with biological targets, Pefloxacin-[d3] unlocks a realm of detailed exploration. By evaluating the binding affinity and functionality of this deuterated compound, researchers unravel the intricate mechanisms of action and resistance, paving the way for the development of potent and selective antibacterial agents.
Toxicological Assessments: Pefloxacin-[d3] finds utility in toxicology studies aimed at assessing the safety profile of pefloxacin. The stable isotope furnishes insights into the drug's distribution, accumulation, and elimination across diverse tissues. These assessments play a pivotal role in forecasting potential side effects and steering safe preclinical usage, safeguarding patient well-being.
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