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-008620 |
Molecular Formula: C8[13C]2H14N15NO4 |
Molecular Weight: 229.21 |
Chemical Structure |
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Description | Porphobilinogen-[13C2,15N] is the isotope labelled analog of Porphobilinogen. Porphobilinogen is an intermediate in the biosynthesis of Heme, found in the urine of patients with acute porphyria. |
Synonyms | 5-(Aminomethyl)-4-(carboxymethyl)-1H-pyrrole-3-propanoic Acid-13C2,15N; PBG-13C2,15N |
Related CAS | 487-90-1 (unlabelled) |
Porphobilinogen-[13C2,15N], a stable isotope-labeled compound, is extensively utilized in biochemical and clinical research. Here are key applications of Porphobilinogen-[13C2,15N] presented with a high degree of perplexity and burstiness:
Metabolic Tracing: Delving into metabolic studies, Porphobilinogen-[13C2,15N] serves as a vital tool for tracing and scrutinizing the flow of intermediates within the heme biosynthesis pathway. By employing isotopically labeled porphobilinogen, researchers can delve into the dynamic interplay of enzyme activities and pathway flux. This insightful information is imperative for unraveling metabolic disorders linked to heme synthesis and for fine-tuning in vitro enzyme assays, unlocking a deeper understanding of biochemical intricacies.
Diagnostic Research: In the realm of clinical research, Porphobilinogen-[13C2,15N] plays a pivotal role in crafting diagnostic assays for the detection and quantification of porphobilinogen in biological samples. Acting as an internal standard in mass spectrometry, it facilitates precise measurements of porphobilinogen levels in conditions such as acute intermittent porphyria. This aids in the prompt diagnosis and effective management of porphyric disorders, emphasizing the importance of accurate and reliable diagnostic tools.
Stable Isotope Assays: Instrumental in stable isotope-labeled assays, this compound is vital for unraveling enzymatic reactions involved in heme production. By analyzing the incorporation of Porphobilinogen-[13C2,15N] into heme, scientists can meticulously monitor enzyme kinetics and the repercussions of genetic mutations on heme synthesis. These assays provide invaluable insights into the molecular underpinnings of heme-related diseases, shedding light on the intricate mechanisms governing cellular processes.
Pharmacokinetic Studies: Porphobilinogen-[13C2,15N] finds application in pharmacokinetic research, where it facilitates the evaluation of drug metabolism and bioavailability impacting heme biosynthesis. By tracking the labeled compound, researchers can assess how pharmaceuticals influence metabolic pathways in vivo, offering crucial insights into drug metabolism and efficacy. This application plays a pivotal role in the development of safer and more efficient therapeutic agents targeting heme metabolism, driving advancements in pharmacological research.
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