Filgotinib Maleate

CHEMBL4298167 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
541.6 g/mol
LogP
Phase
4

This is the maleate salt form of filgotinib, a JAK1-selective inhibitor used to treat inflammatory conditions including rheumatoid arthritis and inflammatory bowel disease. The salt form is used to improve the drug's stability and absorption. It works by suppressing overactive immune signaling pathways that drive chronic inflammation.

分子量

541.6000 g/mol

TPSA

180.00 Ų

治疗领域

作用机制

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

二维结构

SVG PNG

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SMILES

O=C(Nc1nc2cccc(-c3ccc(CN4CCS(=O)(=O)CC4)cc3)n2n1)C1CC1.O=C(O)/C=C\C(=O)O

InChI

InChI=1S/C21H23N5O3S.C4H4O4/c27-20(17-8-9-17)23-21-22-19-3-1-2-18(26(19)24-21)16-6-4-15(5-7-16)14-25-10-12-30(28,29)13-11-25;5-3(6)1-2-4(7)8/h1-7,17H,8-14H2,(H,23,24,27);1-2H,(H,5,6)(H,7,8)/b;2-1-

Molecular Formula

C25H27N5O7S

HBD / HBA

3 / 10

可旋转键数

7

重原子数

38

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

This is the maleate salt form of filgotinib, a JAK1-selective inhibitor used to treat inflammatory conditions including rheumatoid arthritis and inflammatory bowel disease. The salt form is used to improve the drug's stability and absorption. It works by suppressing overactive immune signaling pathways that drive chronic inflammation.

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Yes, Filgotinib Maleate 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). CHEMBL4298167. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 131801100. 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.