Monensin

CHEMBL256105 Phase 4 Approuvé Small molecule

Half-Life

—

Bioavailability

—

Protein Binding

—

Molecular Weight

670.9 g/mol

LogP

4.2

Phase

4

This polyether ionophore antibiotic produced by Streptomyces bacteria disrupts the movement of sodium and potassium ions across cell membranes, giving it activity against certain parasites and bacteria. While primarily used in veterinary medicine and livestock production, it has been investigated for potential anticancer properties.

Masse moléculaire

670,9000 g/mol

LogP

4,20

TPSA

153,00 Å²

Règle des 5 de Lipinski

Non conforme

Aires thérapeutiques

Breast Cancer

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Structure 2D

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SMILES

CC[C@@]1([C@@H]2O[C@@H]([C@H]3O[C@@](O)(CO)[C@H](C)C[C@@H]3C)C[C@@H]2C)CC[C@H]([C@]2(C)CC[C@]3(C[C@H](O)[C@@H](C)[C@@H]([C@@H](C)[C@@H](OC)[C@H](C)C(=O)O)O3)O2)O1

InChI

InChI=1S/C36H62O11/c1-10-34(31-20(3)16-26(43-31)28-19(2)15-21(4)36(41,18-37)46-28)12-11-27(44-34)33(8)13-14-35(47-33)17-25(38)22(5)30(45-35)23(6)29(42-9)24(7)32(39)40/h19-31,37-38,41H,10-18H2,1-9H3,(H,39,40)/t19-,20-,21+,22+,23-,24-,25-,26+,27+,28-,29+,30-,31+,33-,34-,35+,36-/m0/s1

Molecular Formula

C36H62O11

HBD / HBA

4 / 11

Liaisons Rotatives

10

Atomes Lourds

47

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.

Foire aux questions

This polyether ionophore antibiotic produced by Streptomyces bacteria disrupts the movement of sodium and potassium ions across cell membranes, giving it activity against certain parasites and bacteria. While primarily used in veterinary medicine and livestock production, it has been investigated for potential anticancer properties.

Yes, Monensin 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). CHEMBL256105. Open-access bioactivity database.
PubChem — National Center for Biotechnology Information (NCBI). CID 441145. Chemical information database.

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

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Structure

Données Clés

Formule: C36H62O11
Synonymes: 5

Liens externes

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Avertissement médical

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.