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Repositioning Candidate Details

Candidate ID: R0204
Source ID: DB00709
Source Type: approved; investigational
Compound Type: small molecule
Compound Name: Lamivudine
Synonyms:
Molecular Formula: C8H11N3O3S
SMILES: NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1
Structure:
DrugBank 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 Human Immunodeficiency Virus Type 1 (HIV-1) and hepatitis B (HBV).
CAS Number: 134678-17-4
Molecular Weight: 229.256
DrugBank Indication: For the treatment of HIV infection and chronic hepatitis B (HBV).
DrugBank Pharmacology: Lamivudine is a nucleoside reverse transcriptase inhibitor (NRTI) with activity against Human Immunodeficiency Virus Type 1 (HIV-1) and hepatitis B (HBV) to disrupt viral DNA synthesis. When phosphorylated, lamivudine can form active metabolites that compete for incorporation into viral DNA. Via DNA incorporation, lamivudine metabolites competitively inhibit the activity of the HIV reverse transcriptase enzyme and act as a chain terminator of DNA synthesis. Due to the lack of a 3'-OH group, incorporated nucleoside analogues prevent the formation of a 5' to 3' phosphodiester linkage that is essential for DNA chain elongation.
DrugBank MoA: 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.
Targets: Reverse transcriptase/RNaseH; DNA; Protein P
Inclusion Criteria: