Features and properties of remdesivir
| Alternative names | Captisol-enabled remdesivir; Captisol®-enabled GS 5734; GS-5734; Veklury |
| Class | Adenine nucleotides; amines; antivirals; esters; furans; nitriles; phosphorus compounds; pyridazines; pyrroles; small molecules; triazines |
| Mechanism of action | RNA replicase inhibitors |
| Route of administration | Intravenous |
| Pharmacodynamics | Potent and dose-dependent antiviral activity against SARS-CoV-2; therapeutic effects in animal models of SARS-CoV-2 |
| Pharmacokinetics | Undergoes metabolic activation to intracellularly form a pharmacologically active nucleoside analogue triphosphate; predominant circulating metabolite (GS-441524) eliminated via renal clearance |
| Most frequent adverse reactions | |
| Very common (≥ 1/10) | Transaminases increased |
| Common (≥ 1/100 to < 1/10) | Nausea; headache; rash |
| ATC codes | |
| WHO ATC code | J05A-X (other antivirals) |
| EphMRA ATC code | J5B9 (antivirals, others) |
| Chemical name | 2-ethylbutyl ((S)-(((2R,3S,4R,5R)-5-(4-aminopyrrolo[1,2-b]pyridazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphoryl)-L-alaninate |