Mitoxantrone

CHEMBL58 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
444.5 g/mol
LogP
1.0
Phase
4

This chemotherapy and immunosuppressant drug interferes with DNA replication, causing cancer cells and overactive immune cells to die. It is used to treat certain leukemias, breast cancer, and aggressive forms of multiple sclerosis.

Berat Molekul

444,5000 g/mol

LogP

1,00

TPSA

163,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.

Struktur 2D

SVG PNG

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SMILES

O=C1c2c(O)ccc(O)c2C(=O)c2c(NCCNCCO)ccc(NCCNCCO)c21

InChI

InChI=1S/C22H28N4O6/c27-11-9-23-5-7-25-13-1-2-14(26-8-6-24-10-12-28)18-17(13)21(31)19-15(29)3-4-16(30)20(19)22(18)32/h1-4,23-30H,5-12H2

Molecular Formula

C22H28N4O6

HBD / HBA

8 / 10

Ikatan yang Dapat Dirotasi

12

Atom Berat

32

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.

Pertanyaan yang Sering Diajukan

This chemotherapy and immunosuppressant drug interferes with DNA replication, causing cancer cells and overactive immune cells to die. It is used to treat certain leukemias, breast cancer, and aggressive forms of multiple sclerosis.

Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.

Yes, Mitoxantrone 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). CHEMBL58. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4212. Chemical information database.

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

Penyangkalan Medis

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.