Deflazacort

CHEMBL1201891 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
441.5 g/mol
LogP
2.0
Phase
4

A synthetic oxazoline glucocorticoid derived from prednisolone, used as an anti-inflammatory and immunosuppressant and specifically approved for Duchenne muscular dystrophy in the United States. It is considered to have a better safety profile regarding bone loss and weight gain compared to equivalent doses of prednisone.

Berat Molekul

441,5000 g/mol

LogP

2,00

TPSA

102,00 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

CC(=O)OCC(=O)[C@@]12N=C(C)O[C@@H]1C[C@H]1[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]12C

InChI

InChI=1S/C25H31NO6/c1-13-26-25(20(30)12-31-14(2)27)21(32-13)10-18-17-6-5-15-9-16(28)7-8-23(15,3)22(17)19(29)11-24(18,25)4/h7-9,17-19,21-22,29H,5-6,10-12H2,1-4H3/t17-,18-,19-,21+,22+,23-,24-,25+/m0/s1

Molecular Formula

C25H31NO6

HBD / HBA

1 / 7

Ikatan yang Dapat Dirotasi

4

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

A synthetic oxazoline glucocorticoid derived from prednisolone, used as an anti-inflammatory and immunosuppressant and specifically approved for Duchenne muscular dystrophy in the United States. It is considered to have a better safety profile regarding bone loss and weight gain compared to equivalent doses of prednisone.

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

Yes, Deflazacort 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). CHEMBL1201891. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 189821. Chemical information database.

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

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.