Monensin

CHEMBL256105 Phase 4 ได้รับการอนุมัติ 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.

น้ำหนักโมเลกุล

670.9000 g/mol

LogP

4.20

TPSA

153.00 Ų

Lipinski RO5

ไม่ผ่าน

ด้านการรักษา

Pharmacokinetics (PK)

Pharmacodynamics (PD)

โครงสร้าง 2 มิติ

SVG PNG

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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

พันธะที่หมุนได้

10

อะตอมหนัก

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.

คำถามที่พบบ่อย

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.

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.