Filgotinib

CHEMBL3301607 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
425.5 g/mol
LogP
1.4
Phase
4

This oral medication belongs to a class called JAK inhibitors, which work by blocking specific proteins involved in the inflammatory process. It is used to treat moderate-to-severe rheumatoid arthritis and inflammatory bowel disease in adults who have not responded adequately to other treatments. It helps reduce joint pain, swelling, and digestive inflammation.

分子量

425.5000 g/mol

LogP

1.40

TPSA

105.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

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

2D構造

SVG PNG

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SMILES

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

InChI

InChI=1S/C21H23N5O3S/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/h1-7,17H,8-14H2,(H,23,24,27)

Molecular Formula

C21H23N5O3S

HBD / HBA

1 / 6

回転可能結合数

5

重原子数

30

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.

よくある質問

This oral medication belongs to a class called JAK inhibitors, which work by blocking specific proteins involved in the inflammatory process. It is used to treat moderate-to-severe rheumatoid arthritis and inflammatory bowel disease in adults who have not responded adequately to other treatments. It helps reduce joint pain, swelling, and digestive inflammation.

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

Yes, Filgotinib 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). CHEMBL3301607. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 49831257. Chemical information database.

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

医学的免責事項

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.