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 Lamivudine Chemical Structure Lamivudine

Catalog NO.: API-001 | CAS NO.: 134678-17-4 | Brand: BIOCAXIS

Category

Nucleosides & Nucleotides, 2’-deoxy

Synonyms:

Epivir; Zeffix; Heptovir

 2′,3′-Dideoxy-3′-thiacytidine, 3TC

Molecular Formula

C8H11N3O3S

Molecular Weight

229.26

 

General description

Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS.

 Lamivudine has been used to deplete the Hepatitis B Virus (HBV) covalently closed circular DNA (cccDNA) forms for the preparation of inverse nested PCR.

Biochem/physiol Actions

Lamivudine is a potent nucleoside analog reverse transcriptase inhibitor (nRTI).

Lamivudine is a potent nucleoside analog reverse transcriptase inhibitor (nRTI). It is an analogue of cytidine, and can inhibit both types (1 and 2) of HIV reverse transcriptase as well as the reverse transcriptase of hepatitis B. It needs to be phosphorylated to its triphosphate form before it is active. 3TC-triphosphate also inhibits cellular DNA polymerase.

Lamivudine, a synthetic nucleoside analogue, plays a role in the study of viral replication mechanisms, particularly within the context of HIV and Hepatitis B viruses. As a potent inhibitor of reverse transcriptase, an enzyme pivotal for the transcription of viral RNA into DNA, Lamivudine integrates into the viral DNA chain during replication. This incorporation results in chain termination, effectively halting the viruss ability to replicate. Its mechanism underscores the dynamic interplay between viral enzymes and nucleoside analogues, offering a window into understanding viral resistance and the evolution of antiviral strategies. In research, Lamivudine serves as a tool to dissect the complexities of viral life cycles, providing insights into the molecular underpinnings of viral persistence and the development of resistance, thereby contributing to the broader field of antiviral drug discovery and the quest for more effective treatments for viral infections.

 

 

 

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