Fruquintinib

CHEMBL4303214 Phase 4 Đã phê duyệt 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.

Khối lượng phân tử

393,4000 g/mol

LogP

3,40

TPSA

95,70 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

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

Cấu trúc 2D

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

Liên kết có thể quay

5

Nguyên tử nặng

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.

Câu hỏi thường gặp

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.

{# 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). 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.

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.