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Terfenadine-[d3]

General Information
Catalog: BLP-004586
CAS: 192584-82-0
Molecular Formula: C32H38D3NO2
Molecular Weight: 474.69
Chemical Structure
Terfenadine-[d3]
Description Terfenadine-[d3] is a deuterated form of Terfenadine, which is a potent open-channel blocker of hERG (IC50=204 nM), formerly used for the treatment of allergic conditions.
Synonyms α-[4-(1,1-Dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutan-α,β,β-d3-ol; α-[4-(1,1-Dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutanol-d3; α-(p-tert-Butylphenyl)-4-(α-hydroxy-α-phenylbenzyl)-1-piperidinebutanol-d3; Allerplus-d3; Cyater-d3; Histadin-d3; NSC 665802-d3; (±)-Terfenadine-d3
Related CAS 50679-08-8 (unlabelled)

Terfenadine-[d3], a deuterated variant of the antihistamine terfenadine, finds its niche in research applications thanks to its stable isotopic labeling. Here are key applications of Terfenadine-[d3] presented with a high degree of perplexity and burstiness:

Pharmacokinetic Studies: Terfenadine-[d3] plays a pivotal role in pharmacokinetic investigations, shedding light on the absorption, distribution, metabolism, and excretion (ADME) of terfenadine within biological systems. By monitoring the deuterated compound, researchers can distinguish it from endogenous molecules, enabling precise quantification of drug concentrations in diverse biological matrices. This insight aids in optimizing dosing strategies and enhancing drug safety profiles through meticulous examination of drug behavior.

Metabolomics Research: Within the realm of metabolomics, Terfenadine-[d3] emerges as a crucial internal standard and tracer for analytical endeavors. Its stable isotopic labeling offers a distinct signal for identifying and quantifying metabolites in intricate biological samples, enhancing the accuracy of data interpretation. Researchers leverage its capabilities to explore metabolic pathways modulated by terfenadine and investigate potential drug interactions, illuminating the intricate interplay between various compounds within biological systems.

Drug Interaction Studies: Terfenadine-[d3] serves as a valuable tool in elucidating possible drug interactions, enabling scientists to trace its metabolic pathway in the presence of other substances. Its isotopic label acts as a discernible marker for comparative analysis with non-labeled terfenadine, facilitating the examination of the impact of enzyme inhibitors or inducers on drug metabolism. This information proves critical in unraveling the complexities of how different medications or compounds may influence terfenadine's metabolic fate, enhancing our understanding of drug synergies and potential risks.

Analytical Method Development: In the realm of pharmaceutical analysis, Terfenadine-[d3] takes center stage in the development and validation of analytical techniques for detecting terfenadine in pharmaceutical formulations and biological fluids. Its established concentration and stability serve as a benchmark for method calibration and quality control, ensuring the precise determination of terfenadine levels in clinical and research environments. These methodologies play a pivotal role in guaranteeing the accuracy and reliability of terfenadine analysis, underpinning the advancement of pharmaceutical research and clinical practice.

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