Erdafitinib
This oral medication blocks FGFR enzymes that are mutated or overactive in certain cancers, slowing tumor cell growth and division. It is approved for the treatment of FGFR-altered urothelial carcinoma.
Molecular Weight
446.5000 g/mol
LogP
3.20
TPSA
77.30 Ų
Lipinski RO5
Pass
Therapeutic Areas
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D Structure
Cite this structure
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SMILES
COc1cc(OC)cc(N(CCNC(C)C)c2ccc3ncc(-c4cnn(C)c4)nc3c2)c1
InChI
InChI=1S/C25H30N6O2/c1-17(2)26-8-9-31(20-10-21(32-4)13-22(11-20)33-5)19-6-7-23-24(12-19)29-25(15-27-23)18-14-28-30(3)16-18/h6-7,10-17,26H,8-9H2,1-5H3
Molecular Formula
C25H30N6O2
HBD / HBA
1 / 7
Rotatable Bonds
9
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
This oral medication blocks FGFR enzymes that are mutated or overactive in certain cancers, slowing tumor cell growth and division. It is approved for the treatment of FGFR-altered urothelial carcinoma.
Yes, Erdafitinib 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). CHEMBL3545376. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 67462786. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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