Dexrazoxane Hydrochloride
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.
分子量
304.7300 g/mol
TPSA
98.80 Ų
治療領域
作用機序
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)
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.
2D構造
Cite this structure
Embed this structure
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
回転可能結合数
3
重原子数
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.
よくある質問
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
- 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.
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