Suxibuzone

CHEMBL1414320 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
438.5 g/mol
LogP
3.6
Phase
4

Suxibuzone is a prodrug of phenylbutazone, a pyrazolidine-class NSAID, which is hydrolyzed in the body to the active metabolite phenylbutazone and ketobutazone, used for anti-inflammatory and analgesic treatment of musculoskeletal conditions and arthritis. The prodrug form was developed to reduce the gastrointestinal irritation associated with phenylbutazone by providing slower release of the active drug. Like phenylbutazone, it inhibits cyclooxygenase enzymes and has additional effects on leukocyte migration.

分子量

438.5000 g/mol

LogP

3.60

TPSA

104.00 Ų

Lipinski 五规则

符合

作用机制

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

二维结构

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SMILES

CCCCC1(COC(=O)CCC(=O)O)C(=O)N(c2ccccc2)N(c2ccccc2)C1=O

InChI

InChI=1S/C24H26N2O6/c1-2-3-16-24(17-32-21(29)15-14-20(27)28)22(30)25(18-10-6-4-7-11-18)26(23(24)31)19-12-8-5-9-13-19/h4-13H,2-3,14-17H2,1H3,(H,27,28)

Molecular Formula

C24H26N2O6

HBD / HBA

1 / 6

可旋转键数

11

重原子数

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.

常见问题

Suxibuzone is a prodrug of phenylbutazone, a pyrazolidine-class NSAID, which is hydrolyzed in the body to the active metabolite phenylbutazone and ketobutazone, used for anti-inflammatory and analgesic treatment of musculoskeletal conditions and arthritis. The prodrug form was developed to reduce the gastrointestinal irritation associated with phenylbutazone by providing slower release of the active drug. Like phenylbutazone, it inhibits cyclooxygenase enzymes and has additional effects on leukocyte migration.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Suxibuzone 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). CHEMBL1414320. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5362. Chemical information database.

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

医疗免责声明

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.