Antiviral Drug Targets & MOA - Viral Entry & Exit Experts
- Viral Entry Inhibitors: Prevent viral access to host cells.
- Attachment: Maraviroc (HIV; CCR5 antagonist).
- Fusion: Enfuvirtide (HIV; gp41 inhibitor); Docosanol (HSV).

- Viral Release Inhibitors: Block virion exit from infected cells.
- Neuraminidase Inhibitors (Influenza A/B): Oseltamivir, Zanamivir.
- Trap virions by preventing sialic acid cleavage.
⭐ Maraviroc requires a tropism test before use to confirm CCR5-tropic HIV.
- Neuraminidase Inhibitors (Influenza A/B): Oseltamivir, Zanamivir.
Anti-Herpes & Anti-Influenza Drugs - Cold Sore & Cough Crushers

⭐ Acyclovir: viral TK for initial phosphorylation; selective. Resistance: TK mutations.
Anti-Herpes Agents:
- Acyclovir, Valacyclovir:
- MOA: Guanosine analog; viral TK → DNA pol inhibitor.
- Uses: HSV, VZV.
- AE: Crystalline nephropathy.
- Ganciclovir, Valganciclovir:
- MOA: Viral UL97 (CMV) activation.
- Uses: CMV retinitis.
- AE: Myelosuppression. 📌 "Gan-cyc-LOW-vir".
- Foscarnet:
- MOA: Direct DNA pol inhibitor; no activation.
- Uses: Resistant HSV, VZV, CMV.
- AE: Nephrotoxic, electrolytes ↓.
- Cidofovir:
- MOA: Nucleotide analog; DNA pol inhibitor.
- Uses: Resistant CMV.
- AE: Nephrotoxic (w/ Probenecid).
Anti-Influenza Agents:
- Neuraminidase Inhibitors (NAIs): Oseltamivir (PO), Zanamivir (inhaled), Peramivir (IV).
- MOA: Prevents virion release.
- Uses: Flu A/B (start <48h).
- AE: Oseltamivir: GI; Zanamivir: bronchospasm.
- Baloxavir marboxil:
- MOA: Endonuclease inhibitor (mRNA block).
- Uses: Flu A/B (single dose).
Anti-Hepatitis (HBV & HCV) Drugs - Liver's Viral Vanquishers
- Hepatitis B (HBV) - Chronic Management:
- NRTIs (Nucleos(t)ide Analogs):
- Preferred: Tenofovir (TDF/TAF), Entecavir.
- MOA: Inhibit HBV DNA polymerase.
- Tenofovir: TDF (nephrotoxic, ↓bone density); TAF (safer).
- Entecavir: Potent, high resistance barrier.
- Pegylated Interferon alfa-2a (Peg-IFNα):
- MOA: Immunomodulator. Finite (48 wks) therapy.
- S/E: Flu-like, depression, cytopenias.
- NRTIs (Nucleos(t)ide Analogs):
- Hepatitis C (HCV) - Direct-Acting Antivirals (DAAs):
- Classes (📌 HCV DAAs: -previr, -asvir, -buvir):
- NS3/4A Protease-I (-previr): e.g., Glecaprevir.
- NS5A-I (-asvir): e.g., Velpatasvir.
- NS5B Polymerase-I (-buvir): e.g., Sofosbuvir.
- Pangenotypic regimens (e.g., Sofosbuvir/Velpatasvir, Glecaprevir/Pibrentasvir) offer >95% SVR (cure).
- Well-tolerated; short duration (8-12 wks).
- Classes (📌 HCV DAAs: -previr, -asvir, -buvir):

⭐ Sofosbuvir (HCV NS5B inhibitor) is pangenotypic; ⚠️ contraindicated with amiodarone due to risk of severe symptomatic bradycardia.
Antiretroviral Drugs (ART for HIV) - HIV's Resistance Wreckers
-
Goal: Suppress HIV, restore immunity, prevent transmission.
-
Regimen: Typically 2 NRTIs + 1 INSTI.
-
NRTIs (Nucleoside/Nucleotide Reverse Transcriptase Inhibitors): Zidovudine (AZT), Lamivudine (3TC), Abacavir (ABC), Tenofovir (TDF/TAF), Emtricitabine (FTC).
- MoA: Chain termination by inhibiting reverse transcriptase.
- 📌 SE: Lactic acidosis. AZT: Anemia. TDF: Nephrotoxic, bone loss. ABC: Hypersensitivity (test HLA-B*5701).
-
NNRTIs (Non-Nucleoside Reverse Transcriptase Inhibitors): Efavirenz (EFV), Nevirapine (NVP), Rilpivirine (RPV).
- MoA: Allosteric inhibition of reverse transcriptase.
- SE: Rash (SJS/TEN), hepatotoxicity. EFV: CNS effects.
-
PIs (Protease Inhibitors): Atazanavir (ATV), Darunavir (DRV), Lopinavir/Ritonavir (LPV/r).
- MoA: Inhibit HIV protease, preventing viral maturation.
- SE: Metabolic syndrome (hyperlipidemia, hyperglycemia), lipodystrophy. Ritonavir boosts (CYP3A4 inhibitor).
-
INSTIs (Integrase Strand Transfer Inhibitors): Raltegravir (RAL), Dolutegravir (DTG), Bictegravir (BIC).
- MoA: Block integrase, preventing viral DNA integration.
- SE: Generally well-tolerated. DTG: ↑creatinine (benign), rare insomnia/neural tube defect risk.
-
Entry Inhibitors:
- Fusion Inhibitor: Enfuvirtide (binds gp41).
- CCR5 Antagonist: Maraviroc (blocks CCR5; tropism test needed).

⭐ Preferred initial ART for most treatment-naive adults: 2 NRTIs (e.g., Tenofovir alafenamide/Emtricitabine or Abacavir/Lamivudine) + 1 INSTI (e.g., Dolutegravir or Bictegravir).
High‑Yield Points - ⚡ Biggest Takeaways
- Acyclovir: Guanosine analog, activated by viral thymidine kinase. DOC for HSV & VZV. Risk of nephrotoxicity.
- Ganciclovir: Preferred for CMV retinitis. Major side effect: myelosuppression.
- Foscarnet: Treats resistant CMV/HSV. Causes nephrotoxicity, electrolyte imbalance.
- Oseltamivir/Zanamivir: Neuraminidase inhibitors for Influenza A & B treatment and prophylaxis.
- Ribavirin: For chronic Hepatitis C (with DAAs), RSV. Teratogenic, hemolytic anemia.
- Tenofovir/Entecavir: Key NRTIs for Hepatitis B. Sofosbuvir (DAA) for pangenotypic Hepatitis C.
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