Tafamidis Meglumine

CHEMBL2105675 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
503.3 g/mol
LogP
Phase
4

Tafamidis meglumine is the meglumine salt form of tafamidis, a transthyretin stabilizer approved for the treatment of cardiomyopathy caused by hereditary and wild-type transthyretin amyloidosis. See tafamidis for complete pharmacological details.

Molecular Weight

503.3000 g/mol

TPSA

177.00 Ų

Mechanism of Action

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)

Mechanism

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

2D Structure

SVG PNG

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SMILES

CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.O=C(O)c1ccc2nc(-c3cc(Cl)cc(Cl)c3)oc2c1

InChI

InChI=1S/C14H7Cl2NO3.C7H17NO5/c15-9-3-8(4-10(16)6-9)13-17-11-2-1-7(14(18)19)5-12(11)20-13;1-8-2-4(10)6(12)7(13)5(11)3-9/h1-6H,(H,18,19);4-13H,2-3H2,1H3/t;4-,5+,6+,7+/m.0/s1

Molecular Formula

C21H24Cl2N2O8

HBD / HBA

7 / 10

Rotatable Bonds

8

Heavy Atoms

33

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.

Frequently Asked Questions

Tafamidis meglumine is the meglumine salt form of tafamidis, a transthyretin stabilizer approved for the treatment of cardiomyopathy caused by hereditary and wild-type transthyretin amyloidosis. See tafamidis for complete pharmacological details.

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

Yes, Tafamidis Meglumine 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). CHEMBL2105675. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 24970412. Chemical information database.

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

Medical Disclaimer

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.