Aciclovir (ACV), also known as acyclovir and acycloguanosine, is an antiviral medication.[3] It is primarily used for the treatment of herpes simplex virus infections, chickenpox, and shingles. Other uses include prevention of cytomegalovirus infections following transplant and infections due to Epstein-Barr virus. It is available by mouth and intravenously.[4]
Starting at
2-Amino-1,9-dihydro-9-((2-hydroxyethoxy)methyl)-6H-purin-6-one |
Pronunciation | /eɪˈsaɪkloʊvɪər/ |
Trade names | Zovirax, others[1] |
AHFS/Drugs.com | monograph |
MedlinePlus | a681045 |
Licence data | US FDA:link |
Pregnancy category |
AU: B3 |
Legal status |
AU: S4 (Prescription only) for tablet and injection. Unscheduled for cream form under 10 g. CA: ℞-only UK: POM (Prescription only) for tablet and injection. GSL (OTC) for cream form under 2 g. US: ℞-only |
Routes of administration |
Intravenous, oral, topical (including eye ointment) |
Bioavailability | 15–20% (oral)[2] |
Protein binding | 9–33%[2] |
Metabolism | Hepatic |
Biological half-life | 2-4 hours |
Excretion | Renal (62-90% as unchanged drug) |
CAS Number | 59277-89-3 |
ATC code | J05AB01 D06BB03 S01AD03 |
PubChem | CID: 2022 |
IUPHAR/BPS | 4829 |
DrugBank | DB00787 |
ChemSpider | 1945 |
UNII | X4HES1O11F |
KEGG | D00222 |
ChEBI | CHEBI:2453 |
ChEMBL | CHEMBL184 |
Synonyms | acycloguanosine |
PDB ligand ID | AC2 (PDBe, RCSB PDB) |
Formula | C8H11N5O3 |
Molecular mass | 225.21 g·mol−1 |
SMILES[show] |
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InChI[show] |
Melting point | 256.5 °C (493.7 °F) |