Dexrazoxane Hydrochloride

CHEMBL1200778 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
304.7 g/mol
LogP
Phase
4

The hydrochloride salt form of dexrazoxane used intravenously to protect the heart against anthracycline chemotherapy–related cardiotoxicity. It acts as an iron chelator to reduce free radical generation in cardiac tissue.

Berat Molekul

304,7300 g/mol

TPSA

98,80 Ų

Area Terapeutik

Mekanisme Kerja

Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.

Struktur 2D

SVG PNG

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SMILES

C[C@@H](CN1CC(=O)NC(=O)C1)N1CC(=O)NC(=O)C1.Cl

InChI

InChI=1S/C11H16N4O4.ClH/c1-7(15-5-10(18)13-11(19)6-15)2-14-3-8(16)12-9(17)4-14;/h7H,2-6H2,1H3,(H,12,16,17)(H,13,18,19);1H/t7-;/m0./s1

Molecular Formula

C11H17ClN4O4

HBD / HBA

3 / 6

Ikatan yang Dapat Dirotasi

3

Atom Berat

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.

Pertanyaan yang Sering Diajukan

The hydrochloride salt form of dexrazoxane used intravenously to protect the heart against anthracycline chemotherapy–related cardiotoxicity. It acts as an iron chelator to reduce free radical generation in cardiac tissue.

Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.

Yes, Dexrazoxane Hydrochloride 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). CHEMBL1200778. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6918223. Chemical information database.

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

Penyangkalan Medis

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.