Ruxolitinib

CHEMBL1789941 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
306.4 g/mol
LogP
2.1
Phase
4

A JAK1/JAK2 inhibitor used to treat myelofibrosis, polycythemia vera, and steroid-refractory graft-versus-host disease, and as a topical cream for atopic dermatitis and vitiligo. It reduces the overactive inflammatory signaling pathway that drives these conditions.

Masse moléculaire

306,4000 g/mol

LogP

2,10

TPSA

83,20 Ų

Règle des 5 de Lipinski

Conforme

Aires thérapeutiques

Mécanisme d'action

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

Structure 2D

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SMILES

N#CC[C@H](C1CCCC1)n1cc(-c2ncnc3[nH]ccc23)cn1

InChI

InChI=1S/C17H18N6/c18-7-5-15(12-3-1-2-4-12)23-10-13(9-22-23)16-14-6-8-19-17(14)21-11-20-16/h6,8-12,15H,1-5H2,(H,19,20,21)/t15-/m1/s1

Molecular Formula

C17H18N6

HBD / HBA

1 / 4

Liaisons Rotatives

4

Atomes Lourds

23

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.

Foire aux questions

A JAK1/JAK2 inhibitor used to treat myelofibrosis, polycythemia vera, and steroid-refractory graft-versus-host disease, and as a topical cream for atopic dermatitis and vitiligo. It reduces the overactive inflammatory signaling pathway that drives these conditions.

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

Yes, Ruxolitinib 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). CHEMBL1789941. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 25126798. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Avertissement médical

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.