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Description: A reverse transcriptase inhibitor and zalcitabine analog in which a sulfur atom replaces the 3' carbon of the pentose ring. It is used to treat HIV disease. [PubChem]
Drug Type: Small Molecule; Approved; Investigational
Pharmacology: Lamivudine is a nucleoside reverse transcriptase inhibitor (NRTI) with activity against Human Immunodeficiency Virus Type 1 (HIV-1) and hepatitis B (HBV). Lamivudine is phosphorylated to active metabolites that compete for incorporation into viral DNA. They inhibit the HIV reverse transcriptase enzyme competitively and act as a chain terminator of DNA synthesis. The lack of a 3'-OH group in the incorporated nucleoside analogue prevents the formation of the 5' to 3' phosphodiester linkage essential for DNA chain elongation, and therefore, the viral DNA growth is terminated.
Mechanism of Action: Lamivudine is a synthetic nucleoside analogue and is phosphorylated intracellularly to its active 5'-triphosphate metabolite, lamivudine triphosphate (L-TP). This nucleoside analogue is incorporated into viral DNA by HIV reverse transcriptase and HBV polymerase, resulting in DNA chain termination.
Indication: For the treatment of HIV infection and chronic hepatitis B (HBV).
Half Life: 5 to 7 hours
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Thought leaders and organizations working on research involving lamivudine.

  • E Jenny Heathcote
  • Nancy Leung
  • Yun-Fan Liaw
  • Ching-Lung Lai
  • Stefan Zeuzem
  • National Institute of Allergy and Infectious Diseases (NIAID)
  • Idenix Pharmaceuticals
  • Bristol-Myers Squibb
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDD…
  • Glaxo Wellcome
  • University of Hong Kong
  • Chang Gung University College of Medicine
  • National Institute of Diabetes and Digestive and Kidney Diseases
  • University of Milan
  • Chang Gung Memorial Hospital

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