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-004406 |
CAS: 235792-98-0 |
Molecular Formula: C12H13D2N |
Molecular Weight: 175.27 |
Chemical Structure |
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Description | L-Deprenyl-[d2] Precursor is the labelled analogue of (αS)-N-Demethyl Deprenyl, a compound useful in organic synthesis. |
Synonyms | (S)-N-Desmethyl Selegiline-d2; (S)-N-(1-phenylpropan-2-yl)prop-2-yn-1-amine-d2; (αS)-N-Demethyl Deprenyl-d2 |
IUPAC Name | N-(1-phenylpropan-2-yl)prop-2-yn-1,1-d2-1-amine |
Related CAS | 56862-30-7 (unlabelled) |
L-Deprenyl-[d2] Precursor, a deuterated derivative of a crucial synthesis precursor for L-Deprenyl, a versatile pharmaceutical compound, finds diverse clinical and research applications. Here are key applications of L-Deprenyl-[d2] Precursor, presented with a high degree of perplexity and burstiness:
Pharmaceutical Development: In the dynamic realm of pharmaceuticals, L-Deprenyl-[d2] Precursor plays a pivotal role in shaping the development of deuterated L-Deprenyl compounds. This compound is instrumental in optimizing the pharmacokinetic properties of drugs utilized in combating neurodegenerative diseases like Parkinson's and Alzheimer's. Through the strategic substitution of hydrogen with deuterium, the stability and metabolic trajectory of therapeutic compounds can be augmented, potentially ushering in enhanced efficacy and mitigated adverse effects.
Neuroscience Research: Unraveling the complexities of brain function, L-Deprenyl-[d2] Precursor emerges as a crucial instrument in neuroscience research. It unravels the intricate biochemical pathways underpinning neuroprotection and neurotoxicity, shedding light on the crucial role of monoamine oxidase-B (MAO-B) inhibitors in preserving dopamine levels. This compound serves as a conduit for understanding the implications of MAO-B inhibition in the aging process and neurodegenerative conditions, providing valuable insights into potential therapeutic approaches.
Metabolic Studies: Positioned at the intersection of metabolic research, L-Deprenyl-[d2] Precursor stands as a valuable asset for delving into drug metabolism and kinetics. By integrating deuterium into analyses, scientists can conduct more precise and detailed mass spectrometry studies to elucidate metabolic pathways and interactions. This knowledge is instrumental in unraveling the complexities of drug processing within the body and in formulating compounds with favorable metabolic profiles.
Radiotracer Development: Venturing into the realm of radiochemistry, L-Deprenyl-[d2] Precursor finds its niche in the synthesis of deuterated radiotracers tailored for imaging applications. These radiotracers are utilized in positron emission tomography (PET), providing insights into the quantification and visualization of MAO-B activity in the brain. Such studies play a critical role in diagnosing and understanding various neurological disorders, as well as in evaluating the effectiveness of treatment interventions.
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