Mycophenolate Mofetil

CHEMBL1456 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
433.5 g/mol
LogP
3.2
Phase
4

This immunosuppressant medication is used after organ transplantation to prevent the body from rejecting the new organ. It works by reducing the activity of white blood cells that would otherwise attack the transplanted tissue, and is usually taken alongside other anti-rejection drugs.

分子量

433.5000 g/mol

LogP

3.20

TPSA

94.50 Ų

リピンスキーの五則

適合

治療領域

作用機序

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)

機序

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

2D構造

SVG PNG

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SMILES

COc1c(C)c2c(c(O)c1C/C=C(\C)CCC(=O)OCCN1CCOCC1)C(=O)OC2

InChI

InChI=1S/C23H31NO7/c1-15(5-7-19(25)30-13-10-24-8-11-29-12-9-24)4-6-17-21(26)20-18(14-31-23(20)27)16(2)22(17)28-3/h4,26H,5-14H2,1-3H3/b15-4+

Molecular Formula

C23H31NO7

HBD / HBA

1 / 8

回転可能結合数

10

重原子数

31

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.

よくある質問

This immunosuppressant medication is used after organ transplantation to prevent the body from rejecting the new organ. It works by reducing the activity of white blood cells that would otherwise attack the transplanted tissue, and is usually taken alongside other anti-rejection drugs.

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

Yes, Mycophenolate Mofetil 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). CHEMBL1456. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5281078. Chemical information database.

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

医学的免責事項

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.