Brigatinib

CHEMBL3545311 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
584.1 g/mol
LogP
4.6
Phase
4

A next-generation ALK inhibitor used to treat non-small cell lung cancer in patients whose tumors have an ALK gene rearrangement, particularly those who have progressed on other ALK inhibitors. It is designed to overcome resistance mechanisms and penetrate the brain, where lung cancer frequently spreads. It is taken orally once daily.

分子量

584.1000 g/mol

LogP

4.60

TPSA

85.90 Ų

Lipinski 五规则

符合

治疗领域

作用机制

Inhibits anaplastic lymphoma kinase (ALK), a receptor tyrosine kinase whose rearrangement or mutation drives oncogenic signaling in certain cancers.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Inhibits anaplastic lymphoma kinase (ALK), a receptor tyrosine kinase whose rearrangement or mutation drives oncogenic signaling in certain cancers.

二维结构

SVG PNG

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SMILES

COc1cc(N2CCC(N3CCN(C)CC3)CC2)ccc1Nc1ncc(Cl)c(Nc2ccccc2P(C)(C)=O)n1

InChI

InChI=1S/C29H39ClN7O2P/c1-35-15-17-37(18-16-35)21-11-13-36(14-12-21)22-9-10-24(26(19-22)39-2)33-29-31-20-23(30)28(34-29)32-25-7-5-6-8-27(25)40(3,4)38/h5-10,19-21H,11-18H2,1-4H3,(H2,31,32,33,34)

Molecular Formula

C29H39ClN7O2P

HBD / HBA

2 / 9

可旋转键数

8

重原子数

40

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.

常见问题

A next-generation ALK inhibitor used to treat non-small cell lung cancer in patients whose tumors have an ALK gene rearrangement, particularly those who have progressed on other ALK inhibitors. It is designed to overcome resistance mechanisms and penetrate the brain, where lung cancer frequently spreads. It is taken orally once daily.

Inhibits anaplastic lymphoma kinase (ALK), a receptor tyrosine kinase whose rearrangement or mutation drives oncogenic signaling in certain cancers.

Yes, Brigatinib 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). CHEMBL3545311. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 68165256. Chemical information database.

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

医疗免责声明

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.