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-006608 |
Molecular Formula: C19H21D5O3 |
Molecular Weight: 307.44 |
Chemical Structure |
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Synonyms | 16-Ketodehydroepiandrosterone-2,2,3,4,4-d5 |
IUPAC Name | (3R,10R,13S)-3-hydroxy-10,13-dimethyl-1,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-16H-cyclopenta[a]phenanthrene-16,17(2H)-dione-2,2,3,4,4-d5 |
Purity | 95% by CP; 98% atom D |
Storage | Store at -20°C |
16-Ketodehydroepiandrosterone-[d5], a stable isotopically labeled form of the steroid hormone, finds its place in various scientific research applications. Here are key applications infused with high perplexity and burstiness:
Metabolic Research: Delving into metabolic studies, researchers employ 16-Ketodehydroepiandrosterone-[d5] to trace and quantify steroid metabolism pathways in biological systems. Utilizing this labeled compound enables precise measurement of the metabolic conversion rates and pathways of dehydroepiandrosterone (DHEA). This insight aids in unraveling the intricate roles of DHEA in diverse physiological and pathological conditions.
Pharmacokinetic Studies: In the intricate world of pharmacokinetics, 16-Ketodehydroepiandrosterone-[d5] assumes the role of a tracer, shedding light on the absorption, distribution, metabolism, and excretion (ADME) of DHEA and its derivatives. Leveraging this isotopically labeled version allows researchers to track the dynamic interplay of DHEA-related compounds within the body. This knowledge serves as a cornerstone for crafting effective dosing regimens and groundbreaking therapeutic strategies.
Endocrinology Research: Within the realm of endocrinology research, 16-Ketodehydroepiandrosterone-[d5] emerges as a pivotal tool for investigating the biosynthesis and regulation of steroid hormones. By scrutinizing the conversion of labeled DHEA in steroidogenic tissues, researchers glean insights into hormonal regulation and the endocrine system's response to external stimuli. This understanding lays the foundation for unveiling the impacts of hormonal imbalances on health and disease states.
Analytical Chemistry: Playing a crucial role in analytical chemistry, 16-Ketodehydroepiandrosterone-[d5] acts as an internal standard for quantifying DHEA levels using mass spectrometry-based techniques. The isotopic labeling facilitates precise and accurate determination of DHEA concentrations in complex biological matrices. This application stands as a cornerstone for biomarker discovery and validation across diverse clinical and research landscapes.
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