Acyclovir Sodium

CHEMBL1200380 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
247.2 g/mol
LogP
Phase
4

The intravenous sodium salt form of acyclovir, used in hospital settings to treat severe or life-threatening herpes virus infections, including herpes encephalitis, neonatal herpes, and severe chickenpox in immunocompromised patients. It delivers the same antiviral action as oral acyclovir but at higher concentrations achievable through the bloodstream. Adequate hydration during infusion is important to protect the kidneys from crystallization of the drug.

Molekularmasse

247,1900 g/mol

TPSA

122,00 Ų

Therapeutische Bereiche

Wirkmechanismus

Guanosine analogue inhibiting viral DNA polymerase.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Guanosine analogue inhibiting viral DNA polymerase.

2D-Struktur

SVG PNG

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SMILES

Nc1nc([O-])c2ncn(COCCO)c2n1.[Na+]

InChI

InChI=1S/C8H11N5O3.Na/c9-8-11-6-5(7(15)12-8)10-3-13(6)4-16-2-1-14;/h3,14H,1-2,4H2,(H3,9,11,12,15);/q;+1/p-1

Molecular Formula

C8H10N5NaO3

HBD / HBA

2 / 7

Rotierbare Bindungen

4

Schwere Atome

17

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Häufig gestellte Fragen

The intravenous sodium salt form of acyclovir, used in hospital settings to treat severe or life-threatening herpes virus infections, including herpes encephalitis, neonatal herpes, and severe chickenpox in immunocompromised patients. It delivers the same antiviral action as oral acyclovir but at higher concentrations achievable through the bloodstream. Adequate hydration during infusion is important to protect the kidneys from crystallization of the drug.

Guanosine analogue inhibiting viral DNA polymerase.

Yes, Acyclovir Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200380. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 23665721. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Medizinischer Haftungsausschluss

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.