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-004504 |
Molecular Formula: C713CH9D2N[15N]2O3S |
Molecular Weight: 234.25 |
Chemical Structure |
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Description | Lamivudine-[13C,15N2,d2] is an isotope of Lamivudine, a reverse transcriptase inhibitor. Lamivudine is an antiretroviral medication used to prevent and treat HIV/AIDS. |
Synonyms | 2',3'-Dideoxy-3'-thiacytidine-13C,15N2,d2; 3TC-13C,15N2,d2; Epivir-HBV-13C,15N2,d2; Epivir-13C,15N2,d2; Heptovir-13C,15N2,d2; Zeffix-13C,15N2,d2 |
IUPAC Name | 4-amino-1-[(2R,5S)-2-[dideuterio(hydroxy)methyl]-1,3-oxathiolan-5-yl](2-13C,1,3-15N2)pyrimidin-2-one |
Related CAS | 134678-17-4 (unlabelled) |
Canonical SMILES | C1C(OC(S1)CO)N2C=CC(=NC2=O)N |
InChI | InChI=1S/C8H11N3O3S/c9-5-1-2-11(8(13)10-5)6-4-15-7(3-12)14-6/h1-2,6-7,12H,3-4H2,(H2,9,10,13)/t6-,7+/m0/s1/i3D2,8+1,10+1,11+1 |
InChI Key | JTEGQNOMFQHVDC-YWYGFFCWSA-N |
Purity | 98% by CP |
Lamivudine-[13C,15N2,d2], an isotopically labeled antiviral compound widely utilized in research environments, offers a plethora of applications. Here are the key applications of Lamivudine-[13C,15N2,d2]:
Pharmacokinetic Studies: Delving into the intricate world of pharmacokinetics, Lamivudine-[13C,15N2,d2] serves as a pivotal tool for tracing the absorption, distribution, metabolism, and excretion of the drug. By employing isotopically labeled compounds, researchers can precisely measure drug concentrations in diverse biological matrices, unraveling the drug's behavior within the body and refining dosing regimens with precision.
Bioavailability Assessment: Within the realm of bioavailability studies, Lamivudine-[13C,15N2,d2] plays a crucial role in assessing the extent and speed of absorption of various Lamivudine formulations. The isotopically labeled compound enables meticulous quantification in plasma samples, ensuring robust data on relative bioavailability. This data is essential for shaping new drug formulations and enhancing generic drug development.
Metabolic Pathway Elucidation: Researchers leverage Lamivudine-[13C,15N2,d2] to delve into the intricate metabolic pathways of Lamivudine within the human body. By meticulously tracking the labeled compound through its metabolic conversions, scientists can pinpoint and quantify metabolites. This wealth of knowledge sheds light on the drug's mechanism of action, potential side effects, and interactions with other medications.
Drug Interaction Studies: At the forefront of drug interaction research, Lamivudine-[13C,15N2,d2] emerges as a critical asset in exploring drug-drug interactions. By co-administering the labeled compound with other drugs, researchers unveil how the presence of one drug impacts the pharmacokinetics and metabolism of Lamivudine. This effort enhances the optimization of combination therapies, minimizing adverse interactions, and enhancing preclinical outcomes significantly.
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