Sorivudine

CHEMBL70046 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
349.1 g/mol
LogP
-0.9
Phase
4

Sorivudine is a nucleoside analog with potent antiviral activity against varicella-zoster virus (VZV) and Epstein-Barr virus, used for the treatment of herpes zoster (shingles) and investigated in breast cancer patients with herpes complications. It is phosphorylated by viral thymidine kinase to its active triphosphate form, which selectively inhibits viral DNA polymerase and terminates viral DNA chain elongation. A severe drug interaction with fluorouracil-based chemotherapy limits its use in cancer patients.

Peso molecular

349,1300 g/mol

LogP

-0,90

TPSA

119,00 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Mecanismo de acción

Functions as a nucleoside analog that is incorporated into viral or cellular DNA/RNA during replication, causing chain termination or coding errors that inhibit pathogen proliferation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Functions as a nucleoside analog that is incorporated into viral or cellular DNA/RNA during replication, causing chain termination or coding errors that inhibit pathogen proliferation.

Estructura 2D

SVG PNG

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SMILES

O=c1[nH]c(=O)n([C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)cc1/C=C/Br

InChI

InChI=1S/C11H13BrN2O6/c12-2-1-5-3-14(11(19)13-9(5)18)10-8(17)7(16)6(4-15)20-10/h1-3,6-8,10,15-17H,4H2,(H,13,18,19)/b2-1+/t6-,7-,8+,10-/m1/s1

Molecular Formula

C11H13BrN2O6

HBD / HBA

4 / 6

Enlaces Rotables

3

Átomos Pesados

20

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.

Preguntas frecuentes

Sorivudine is a nucleoside analog with potent antiviral activity against varicella-zoster virus (VZV) and Epstein-Barr virus, used for the treatment of herpes zoster (shingles) and investigated in breast cancer patients with herpes complications. It is phosphorylated by viral thymidine kinase to its active triphosphate form, which selectively inhibits viral DNA polymerase and terminates viral DNA chain elongation. A severe drug interaction with fluorouracil-based chemotherapy limits its use in cancer patients.

Functions as a nucleoside analog that is incorporated into viral or cellular DNA/RNA during replication, causing chain termination or coding errors that inhibit pathogen proliferation.

Yes, Sorivudine 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). CHEMBL70046. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5282192. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso médico

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.