Trientine

CHEMBL609 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
146.2 g/mol
LogP
-2.5
Phase
4

Trientine (triethylenetetramine, TETA) is a polyamine copper-chelating agent that forms stable complexes with copper ions, promoting urinary copper excretion and reducing systemic copper accumulation in Wilson's disease (hepatolenticular degeneration), a genetic disorder of copper metabolism due to ATP7B mutations. It is used as an alternative to penicillamine in patients who are intolerant to or who fail penicillamine therapy. Its chelation of excess hepatic and systemic copper prevents oxidative liver injury and neurological damage characteristic of untreated Wilson's disease.

Khối lượng phân tử

146,2300 g/mol

LogP

-2,50

TPSA

76,10 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

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)

Cơ chế

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.

Cấu trúc 2D

SVG PNG

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SMILES

NCCNCCNCCN

InChI

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

Molecular Formula

C6H18N4

HBD / HBA

4 / 4

Liên kết có thể quay

7

Nguyên tử nặng

10

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.

Câu hỏi thường gặp

Trientine (triethylenetetramine, TETA) is a polyamine copper-chelating agent that forms stable complexes with copper ions, promoting urinary copper excretion and reducing systemic copper accumulation in Wilson's disease (hepatolenticular degeneration), a genetic disorder of copper metabolism due to ATP7B mutations. It is used as an alternative to penicillamine in patients who are intolerant to or who fail penicillamine therapy. Its chelation of excess hepatic and systemic copper prevents oxidative liver injury and neurological damage characteristic of untreated Wilson's disease.

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 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). CHEMBL609. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5565. Chemical information database.

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

Tuyên bố miễn trách y tế

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.