Amifostine

CHEMBL1006 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
214.2 g/mol
LogP
-4.5
Phase
4

A cytoprotective prodrug that is converted to an active metabolite in normal tissues to scavenge free radicals and reduce the toxicity of radiation and certain chemotherapy drugs like cisplatin, protecting healthy cells while having limited activity in tumor tissue. It is used to reduce kidney toxicity from cisplatin and decrease dry mouth from head and neck radiation therapy.

Peso molecular

214,2300 g/mol

LogP

-4,50

TPSA

121,00 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Mecanismo de acción

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Estructura 2D

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SMILES

NCCCNCCSP(=O)(O)O

InChI

InChI=1S/C5H15N2O3PS/c6-2-1-3-7-4-5-12-11(8,9)10/h7H,1-6H2,(H2,8,9,10)

Molecular Formula

C5H15N2O3PS

HBD / HBA

4 / 6

Enlaces Rotables

7

Átomos Pesados

12

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

A cytoprotective prodrug that is converted to an active metabolite in normal tissues to scavenge free radicals and reduce the toxicity of radiation and certain chemotherapy drugs like cisplatin, protecting healthy cells while having limited activity in tumor tissue. It is used to reduce kidney toxicity from cisplatin and decrease dry mouth from head and neck radiation therapy.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Amifostine 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). CHEMBL1006. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2141. Chemical information database.

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

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.