Lamivudine-[13C,15N2,d2] - Isotope / BOC Sciences

General Information
Catalog: BLP-004504
Molecular Formula: C713CH9D2N[15N]2O3S
Molecular Weight: 234.25

General Information

Catalog: BLP-004504

Molecular Formula: C713CH9D2N[15N]2O3S

Molecular Weight: 234.25

Chemical Structure

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.