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-008591 |
Molecular Formula: C19H14D6FNO3.C4H4O4 |
Molecular Weight: 451.50 |
Chemical Structure |
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Description | Paroxetine Maleate-[d6] is the labelled derivative of Paroxetine Maleate. Paroxetine maleate is a selective serotonin uptake inhibitor. |
Synonyms | (3S-trans)-3-[(1,3-Benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)-piperidine (Z)-2-Butenedioate-d6; Paroxetine Maleate-d6 |
Related CAS | 64006-44-6 (unlabelled) |
Purity | 98% by CP; 98% atom D |
Paroxetine Maleate-[d6], a deuterated iteration of Paroxetine, a renowned selective serotonin reuptake inhibitor (SSRI), is utilized widely as an antidepressant. Here are key applications of Paroxetine Maleate-[d6] presented with a high degree of perplexity and burstiness:
Pharmacokinetic Studies: Paroxetine Maleate-[d6] plays a pivotal role in pharmacokinetic studies, offering insights into the absorption, distribution, metabolism, and excretion of Paroxetine within the body. The deuterated signature permits researchers to discern and track the drug amidst biological samples, facilitating the delineation of the drug's bioavailability and systemic exposure, thereby unraveling its intricate pharmacological profile.
Metabolism Research: In the realm of metabolism research, Paroxetine Maleate-[d6] shines as a tool for investigating the metabolic pathways and enzyme interactions governing Paroxetine's biotransformation. The isotopic labeling capability distinguishes metabolites arising from Paroxetine, enabling a meticulous dissection of the metabolic cascade. Researchers can pinpoint the specific enzymes orchestrating drug metabolism, shedding light on drug-drug interactions and the individual variability in drug response.
Analytical Method Development: Serving as an internal standard, Paroxetine Maleate-[d6] aids in the refinement of analytical methods for quantifying Paroxetine across diverse matrices like plasma or urine. Its structural resemblance to Paroxetine, coupled with its distinct isotopic fingerprint, enhances the precision and accuracy of analytical measurements. This precision is critical for therapeutic drug monitoring, ensuring consistent drug dosages in clinical setups.
Drug Stability Studies: Paroxetine Maleate-[d6] emerges as an indispensable asset in assessing the stability of Paroxetine and its formulations under varying conditions. By utilizing this labeled compound, researchers can monitor alterations in the drug's concentration over time and in response to environmental stimuli. A comprehensive understanding of Paroxetine's stability aids in optimizing storage conditions and determining shelf-life for pharmaceutical products, safeguarding drug efficacy and safety.
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