Ganciclovir

Ganciclovir
Clinical data
Pronunciation/ɡænˈskləvɪər/
Trade namesCytovene; Cymevene; Vitrasert
Other namesgancyclovir; DHPG; 9-(1,3-dihydroxy-2-propoxymethyl)guanine
AHFS/Drugs.comMonograph
MedlinePlusa605011
License data
Pregnancy
category
  • AU: D
Routes of
administration
Intravenous, by mouth, intravitreal
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability5% (oral)
Metabolismguanylate kinase (CMV UL97 gene product)
Elimination half-life2.5–5 hours
ExcretionKidney
Identifiers
  • 2-Amino-9-(1,3-dihydroxypropan-2-yloxymethyl)-3H-purin-6-one
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.155.403 Edit this at Wikidata
Chemical and physical data
FormulaC9H13N5O4
Molar mass255.234 g·mol−1
3D model (JSmol)
Melting point250 °C (482 °F) (dec.)
  • O=C2/N=C(\Nc1n(cnc12)COC(CO)CO)N
  • InChI=1S/C9H13N5O4/c10-9-12-7-6(8(17)13-9)11-3-14(7)4-18-5(1-15)2-16/h3,5,15-16H,1-2,4H2,(H3,10,12,13,17) checkY
  • Key:IRSCQMHQWWYFCW-UHFFFAOYSA-N checkY
  (verify)

Ganciclovir, sold under the brand name Cytovene among others, is an antiviral medication used to treat cytomegalovirus (CMV) infections.

Ganciclovir was patented in 1980 and approved for medical use in 1988.[4]

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  2. ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 30 March 2024.
  3. ^ "Product monograph brand safety updates". Health Canada. 7 July 2016. Retrieved 13 July 2024.
  4. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 504. ISBN 9783527607495.