Fruquintinib

CHEMBL4303214 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
393.4 g/mol
LogP
3.4
Phase
4

This oral medication inhibits VEGF receptors that promote tumor blood vessel formation, cutting off the blood supply that colorectal and lung tumors need to grow. It is used in later lines of treatment for metastatic colorectal cancer and non-small cell lung cancer that has progressed on prior therapies.

Molecular Weight

393.4000 g/mol

LogP

3.40

TPSA

95.70 Ų

Lipinski RO5

Pass

Therapeutic Areas

Mechanism of Action

Inhibits vascular endothelial growth factor (VEGF) signaling, blocking angiogenesis (new blood vessel formation) that tumors require for growth and metastasis.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Inhibits vascular endothelial growth factor (VEGF) signaling, blocking angiogenesis (new blood vessel formation) that tumors require for growth and metastasis.

2D Structure

SVG PNG

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SMILES

CNC(=O)c1c(C)oc2cc(Oc3ncnc4cc(OC)c(OC)cc34)ccc12

InChI

InChI=1S/C21H19N3O5/c1-11-19(20(25)22-2)13-6-5-12(7-16(13)28-11)29-21-14-8-17(26-3)18(27-4)9-15(14)23-10-24-21/h5-10H,1-4H3,(H,22,25)

Molecular Formula

C21H19N3O5

HBD / HBA

1 / 7

Rotatable Bonds

5

Heavy Atoms

29

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 inhibits VEGF receptors that promote tumor blood vessel formation, cutting off the blood supply that colorectal and lung tumors need to grow. It is used in later lines of treatment for metastatic colorectal cancer and non-small cell lung cancer that has progressed on prior therapies.

Inhibits vascular endothelial growth factor (VEGF) signaling, blocking angiogenesis (new blood vessel formation) that tumors require for growth and metastasis.

Yes, Fruquintinib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4303214. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 44480399. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

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.