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Oclacitinib-[13C,d3]

General Information
Catalog: BLP-003620
Molecular Formula: C14[13C]H20D3N5O2S
Molecular Weight: 341.45
Chemical Structure
Oclacitinib-[13C,d3]
Description Oclacitinib-[13C,d3], is the labelled analogue of Oclacitinib. Oclacitinib is a synthetic cyclohexylamino pyrrolopyrimidine janus kinase inhibitor that is relatively selective for JAK1.
Synonyms Oclacitinib-13C D3
IUPAC Name N-methyl-1-(4-((methyl-13C-d3)(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)cyclohexyl)methanesulfonamide
Related CAS 1208319-26-9 (unlabelled)

Oclacitinib-[13C,d3], a stable isotope-labeled variant of Oclacitinib, serves as a valuable tool in scientific research, particularly in the realms of pharmacokinetics and metabolism. Here, we explore key applications of Oclacitinib-[13C,d3], presented with a high degree of perplexity and burstiness:

Pharmacokinetic Studies: In the realm of pharmacokinetics, Oclacitinib-[13C,d3] plays a pivotal role in tracing the journey of the drug through the body—shedding light on absorption, distribution, metabolism, and excretion processes. The distinctive [13Cd3] labeling distinguishes the administered compound from endogenous substances, providing intricate insights into the drug's behavior within biological systems. This wealth of data proves critical in fine-tuning dosing regimens and optimizing drug efficacy, ultimately shaping the landscape of pharmaceutical interventions.

Metabolic Pathway Elucidation: Delving into metabolic pathways, Oclacitinib-[13C,d3] emerges as a powerhouse, unraveling the intricate biotransformation processes of Oclacitinib. By tracking labeled atoms, researchers unveil metabolic intermediates and end products, offering a comprehensive understanding of the drug's journey within animal models and human subjects. This knowledge not only elucidates potential drug interactions but also sheds light on the formation of metabolites with therapeutic or toxicological implications, paving the way for informed decision-making in drug development.

Clinical Research: The utility of Oclacitinib-[13C,d3] extends into the realm of clinical research, where it serves as an internal standard in mass spectrometry assays for quantifying Oclacitinib concentrations in biological samples. This precise quantification ensures accuracy and reliability in assessing drug levels—crucial for both clinical trials and therapeutic drug monitoring. Through establishing robust pharmacokinetic and pharmacodynamic profiles, Oclacitinib-[13C,d3] plays a pivotal role in navigating the regulatory landscape, shaping the future of pharmaceutical innovations.

Drug Interaction Studies: Oclacitinib-[13C,d3] steps into the spotlight in studies exploring potential drug-drug interactions, offering a unique perspective on how concomitant medications influence the metabolism and efficacy of Oclacitinib. By leveraging the labeled compound, researchers gain valuable insights into the interplay between different drugs, foreseeing adverse interactions and guiding the development of safe co-administration protocols in clinical settings. This nuanced understanding of drug interactions revolutionizes the approach to personalized medicine, paving the way for safer and more effective therapeutic interventions.

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