Tafamidis

CHEMBL2103837 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
308.1 g/mol
LogP
4.2
Phase
4

Tafamidis is a selective transthyretin (TTR) stabilizer that binds to the thyroxine-binding sites of TTR tetramers, preventing their dissociation into monomers and halting the amyloidogenic cascade responsible for transthyretin amyloid cardiomyopathy (ATTR-CM). By kinetically stabilizing the native TTR tetramer, it reduces misfolding and fibril deposition in cardiac tissue, slowing progression of cardiomyopathy. It is the first disease-modifying therapy approved for ATTR-CM and demonstrates mortality reduction in clinical trials.

الوزن الجزيئي

308,1000 g/mol

LogP

4,20

TPSA

63,30 Ų

قاعدة ليبينسكي للخمسة

ناجح

آلية العمل

Stabilizes the transthyretin (TTR) protein tetramer, preventing its dissociation into monomers that misfold and aggregate into amyloid fibrils in cardiac tissue.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

الآلية

Stabilizes the transthyretin (TTR) protein tetramer, preventing its dissociation into monomers that misfold and aggregate into amyloid fibrils in cardiac tissue.

البنية ثنائية الأبعاد

SVG PNG

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SMILES

O=C(O)c1ccc2nc(-c3cc(Cl)cc(Cl)c3)oc2c1

InChI

InChI=1S/C14H7Cl2NO3/c15-9-3-8(4-10(16)6-9)13-17-11-2-1-7(14(18)19)5-12(11)20-13/h1-6H,(H,18,19)

Molecular Formula

C14H7Cl2NO3

HBD / HBA

1 / 4

الروابط القابلة للدوران

2

الذرات الثقيلة

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.

الأسئلة الشائعة

Tafamidis is a selective transthyretin (TTR) stabilizer that binds to the thyroxine-binding sites of TTR tetramers, preventing their dissociation into monomers and halting the amyloidogenic cascade responsible for transthyretin amyloid cardiomyopathy (ATTR-CM). By kinetically stabilizing the native TTR tetramer, it reduces misfolding and fibril deposition in cardiac tissue, slowing progression of cardiomyopathy. It is the first disease-modifying therapy approved for ATTR-CM and demonstrates mortality reduction in clinical trials.

Stabilizes the transthyretin (TTR) protein tetramer, preventing its dissociation into monomers that misfold and aggregate into amyloid fibrils in cardiac tissue.

Yes, Tafamidis 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). CHEMBL2103837. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 11001318. Chemical information database.

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

إخلاء المسؤولية الطبية

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.