Ruxolitinib Phosphate

CHEMBL1795071 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
404.4 g/mol
LogP
Phase
4

The phosphate salt formulation of ruxolitinib used to treat bone marrow disorders including myelofibrosis and polycythemia vera by inhibiting JAK enzymes that drive abnormal blood cell production. It can significantly reduce spleen size and improve quality of life in patients with these conditions.

Molekularmasse

404,4000 g/mol

TPSA

161,00 Ų

Therapeutische Bereiche

Wirkmechanismus

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)

Mechanismus

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

2D-Struktur

SVG PNG

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SMILES

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

InChI

InChI=1S/C17H18N6.H3O4P/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;1-5(2,3)4/h6,8-12,15H,1-5H2,(H,19,20,21);(H3,1,2,3,4)/t15-;/m1./s1

Molecular Formula

C17H21N6O4P

HBD / HBA

4 / 8

Rotierbare Bindungen

4

Schwere Atome

28

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.

Häufig gestellte Fragen

The phosphate salt formulation of ruxolitinib used to treat bone marrow disorders including myelofibrosis and polycythemia vera by inhibiting JAK enzymes that drive abnormal blood cell production. It can significantly reduce spleen size and improve quality of life in patients with 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 Phosphate 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). CHEMBL1795071. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 25127112. Chemical information database.

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

Medizinischer Haftungsausschluss

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.