Oseltamivir Phosphate

CHEMBL1200340 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
410.4 g/mol
LogP
Phase
4

A phosphate salt form of oseltamivir with the same therapeutic properties. An antiviral neuraminidase inhibitor for treating and preventing influenza, most effective within 48 hours.

Khối lượng phân tử

410,4000 g/mol

TPSA

168,00 Ų

Lĩnh vực điều trị

Cơ chế tác dụng

Inhibits viral neuraminidase, preventing the release of newly formed virus particles from infected cells and limiting viral spread within the respiratory tract.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Inhibits viral neuraminidase, preventing the release of newly formed virus particles from infected cells and limiting viral spread within the respiratory tract.

Cấu trúc 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=P(O)(O)O

InChI

InChI=1S/C16H28N2O4.H3O4P/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)18-10(4)19;1-5(2,3)4/h9,12-15H,5-8,17H2,1-4H3,(H,18,19);(H3,1,2,3,4)/t13-,14+,15+;/m0./s1

Molecular Formula

C16H31N2O8P

HBD / HBA

5 / 9

Liên kết có thể quay

8

Nguyên tử nặng

27

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.

Câu hỏi thường gặp

A phosphate salt form of oseltamivir with the same therapeutic properties. An antiviral neuraminidase inhibitor for treating and preventing influenza, most effective within 48 hours.

Inhibits viral neuraminidase, preventing the release of newly formed virus particles from infected cells and limiting viral spread within the respiratory tract.

Yes, Oseltamivir Phosphate 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). CHEMBL1200340. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 78000. Chemical information database.

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

Tuyên bố miễn trách y tế

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.