Trientine Hydrochloride

CHEMBL3989777 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
219.2 g/mol
LogP
Phase
4

Trientine hydrochloride is the hydrochloride salt form of trientine, a copper-chelating agent used for Wilson's disease and under investigation as an anti-fibrotic agent in melanoma through copper-dependent pathways. See trientine for complete pharmacological details. This salt formulation is used in approved oral capsule preparations.

分子量

219.1500 g/mol

TPSA

76.10 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)

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.

2D構造

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SMILES

Cl.Cl.NCCNCCNCCN

InChI

InChI=1S/C6H18N4.2ClH/c7-1-3-9-5-6-10-4-2-8;;/h9-10H,1-8H2;2*1H

Molecular Formula

C6H20Cl2N4

HBD / HBA

6 / 4

回転可能結合数

7

重原子数

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.

よくある質問

Trientine hydrochloride is the hydrochloride salt form of trientine, a copper-chelating agent used for Wilson's disease and under investigation as an anti-fibrotic agent in melanoma through copper-dependent pathways. See trientine for complete pharmacological details. This salt formulation is used in approved oral capsule preparations.

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, Trientine 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). CHEMBL3989777. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 71433. Chemical information database.

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

医学的免責事項

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.