Taurolidine

CHEMBL2105420 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
284.4 g/mol
LogP
-1.7
Phase
4

Taurolidine is a synthetic derivative of the amino acid taurine with broad-spectrum antimicrobial and antineoplastic properties, acting by releasing formaldehyde-like reactive intermediates that disrupt microbial cell walls and induce tumor cell apoptosis. It has been used as a catheter lock solution to prevent catheter-related bloodstream infections and is investigational for various cancers including ovarian cancer. Its dual antimicrobial and antitumor activity makes it a unique agent in oncology.

Berat Molekul

284,4000 g/mol

LogP

-1,70

TPSA

116,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Struktur 2D

SVG PNG

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SMILES

O=S1(=O)CCN(CN2CCS(=O)(=O)NC2)CN1

InChI

InChI=1S/C7H16N4O4S2/c12-16(13)3-1-10(5-8-16)7-11-2-4-17(14,15)9-6-11/h8-9H,1-7H2

Molecular Formula

C7H16N4O4S2

HBD / HBA

2 / 8

Ikatan yang Dapat Dirotasi

2

Atom Berat

17

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

Taurolidine is a synthetic derivative of the amino acid taurine with broad-spectrum antimicrobial and antineoplastic properties, acting by releasing formaldehyde-like reactive intermediates that disrupt microbial cell walls and induce tumor cell apoptosis. It has been used as a catheter lock solution to prevent catheter-related bloodstream infections and is investigational for various cancers including ovarian cancer. Its dual antimicrobial and antitumor activity makes it a unique agent in oncology.

Yes, Taurolidine 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). CHEMBL2105420. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 29566. 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.