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-012531 |
CAS: 1217695-77-6 |
Molecular Formula: C10H14D3N3S |
Molecular Weight: 214.34 |
Chemical Structure |
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Description | Pramipexole-[d3] is the labelled analogue of Pramipexole. Pramipexole is used to treat symptoms of Parkinson's disease (stiffness, tremors, muscle spasms, and poor muscle control). |
Synonyms | Pramipexole D3; (S)-4,5,6,7-Tetrahydro-N6-(propyl-d3)-2,6-benzothiazolediamine Dihydrochloride |
IUPAC Name | (6S)-6-N-(3,3,3-trideuteriopropyl)-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine |
Related CAS | 104632-26-0 (unlabelled free base) |
Canonical SMILES | CCCNC1CCC2=C(C1)SC(=N2)N |
InChI | InChI=1S/C10H17N3S/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8/h7,12H,2-6H2,1H3,(H2,11,13)/t7-/m0/s1/i1D3 |
InChI Key | FASDKYOPVNHBLU-LNEZGBMJSA-N |
Melting Point | >260°C (dec.) |
Purity | 98% by HPLC; 98% atom D |
Solubility | Soluble in Methanol, Water |
Appearance | White to Off-white Solid |
Storage | Store at -20°C, under inert atmosphere |
Pramipexole-[d3], a deuterated variant of the dopamine agonist pramipexole, holds considerable significance in clinical and research domains. Here are the key applications of Pramipexole-[d3]:
Pharmacokinetic Studies: Widely employed in pharmacokinetic investigations, Pramipexole-[d3] facilitates the comprehensive examination of pramipexole's absorption, distribution, metabolism, and excretion within the body. Through leveraging the deuterated form, researchers can discriminate between the drug and its metabolites, shedding light on drug metabolism intricacies and refining dosing strategies. This approach enhances the understanding of drug kinetics and fosters optimal therapeutic approaches.
Neuropharmacology Research: In the realm of neuropharmacology, Pramipexole-[d3] plays a pivotal role in elucidating the mechanisms of action of dopamine agonists. It serves as a crucial tool for exploring how the drug impacts dopamine receptors and neural pathways linked to movement disorders. Such research endeavors hold the promise of advancing treatment modalities for debilitating conditions like Parkinson's disease and restless leg syndrome, unveiling novel therapeutic avenues through nuanced investigations.
Stable Isotope Labeling: Serving as a stable isotope-labeled internal standard in mass spectrometry-based assays, Pramipexole-[d3] stands as a cornerstone for accurately quantifying pramipexole in biological samples with precision and fidelity. By utilizing the labeled compound, researchers can minimize analytical variations, ensuring the reliability and reproducibility of pharmacological studies. This application elevates the standards of quantitative analyses, bolstering the robustness of pharmacokinetic assessments and enhancing the overall accuracy of experimental outcomes.
Brain Imaging Studies: Pramipexole-[d3] finds utility in cutting-edge brain imaging modalities such as positron emission tomography (PET), enabling the visualization and quantification of dopamine receptor binding in vivo. This instrumental in vivo mapping aids in exploring the drug's distribution patterns and receptor occupancy levels within the brain, offering crucial insights into its pharmacological profile and therapeutic efficacy. The application of such imaging techniques is indispensable for optimizing treatment strategies, providing a deeper understanding of drug action mechanisms, and paving the way for tailored therapeutic interventions.
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