Antivirals Flashcards
Adefovir
Nucleotide analogue
Adefovir dipivoxil is metabolised to adefovir diphosphate, a nucleotide analogue of deoxyadenosine monophosphate, which acts as an alternative substrate for viral DNA polymerase resulting in DNA chain termination and prevention of viral DNA synthesis.
Entecavir
Nucleoside analogue
Entecavir is a guanosine analogue; entecavir triphosphate inhibits hepatitis B polymerase, preventing viral DNA synthesis.
Peginterferon alfa‑2a
Inhibits viral replication and has immunomodulatory effects.
Glecaprevir with Pibrentasvir
Inhibits hepatitis C viral replication; glecaprevir is an HCV NS3/4A protease inhibitor and pibrentasvir is an HCV NS5A inhibitor (also prevents assembly of the virus).
Ledipasvir with sofosbuvir
Inhibits hepatitis C viral replication: sofosbuvir is metabolised to active uridine analogue triphosphate and this inhibits HCV NS5B RNA polymerase; ledipasvir inhibits HCV NS5A protein (also prevents assembly of the virus).
Ribavirin
Nucleoside analogue
Nucleoside analogue that interferes with RNA and DNA synthesis, thereby inhibiting protein synthesis and viral replication.
Sofosbuvir
Metabolised to active uridine analogue triphosphate and this inhibits HCV NS5B RNA polymerase, thereby impeding hepatitis C viral replication.
Sofosbuvir with velpatasvir
Inhibits hepatitis C viral replication: sofosbuvir is metabolised to active uridine analogue triphosphate and this inhibits HCV NS5B RNA polymerase; velpatasvir inhibits HCV NS5A protein (also prevents assembly of the virus).
Sofosbuvir with velpatasvir and voxilaprevir
Inhibits hepatitis C viral replication: sofosbuvir is metabolised to active uridine analogue triphosphate and this inhibits HCV NS5B RNA polymerase; velpatasvir inhibits HCV NS5A protein (also prevents assembly of the virus); voxilaprevir inhibits HCV NS3/4A protease.
Abacavir
Purine Nucleoside reverse transcriptase inhibitor
The active phosphorylated NRTI metabolites inhibit viral reverse transcriptase and viral DNA synthesis, preventing HIV replication. The specific site of action differs for each drug; these differences are exploited in combination regimens.
Lamivudine
Pyrimidine Nucleoside reverse transcriptase inhibitor
The active phosphorylated NRTI metabolites inhibit viral reverse transcriptase and viral DNA synthesis, preventing HIV replication. The specific site of action differs for each drug; these differences are exploited in combination regimens.
Tenofovir
Purine Nucleoside reverse transcriptase inhibitor
Tenofovir is metabolised to active tenofovir diphosphate, which inhibits viral polymerases and terminates the DNA chain after incorporation into viral DNA.
Emtricitabine
Pyrimidine Nucleoside reverse transcriptase inhibitor
The active phosphorylated NRTI metabolites inhibit viral reverse transcriptase and viral DNA synthesis, preventing HIV replication. The specific site of action differs for each drug; these differences are exploited in combination regimens.
Zidovudine
Nucleoside reverse transcriptase inhibitor
The active phosphorylated NRTI metabolites inhibit viral reverse transcriptase and viral DNA synthesis, preventing HIV replication. The specific site of action differs for each drug; these differences are exploited in combination regimens.
Etravirine
Non-nucleoside reverse transcriptase inhibitor
NNRTIs reversibly inhibit HIV‑1 reverse transcriptase, reducing viral DNA synthesis.
Nevirapine
Non-nucleoside reverse transcriptase inhibitor
NNRTIs reversibly inhibit HIV‑1 reverse transcriptase, reducing viral DNA synthesis.