Fosnetupitant

CHEMBL3989917 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
688.6 g/mol
LogP
5.0
Phase
4

A prodrug of netupitant, a neurokinin-1 receptor antagonist used to prevent chemotherapy-induced nausea and vomiting, particularly delayed nausea. After intravenous administration, it is rapidly converted to netupitant which blocks substance P from triggering nausea signals in the brain. It is often combined with a 5-HT3 antagonist for broader antiemetic coverage.

Khối lượng phân tử

688,6000 g/mol

LogP

5,00

TPSA

106,00 Ų

Lipinski RO5

Không đạt

Cơ chế tác dụng

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Cấu trúc 2D

SVG PNG

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SMILES

Cc1ccccc1-c1cc(N2CC[N+](C)(COP(=O)([O-])O)CC2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1

InChI

InChI=1S/C31H35F6N4O5P/c1-20-8-6-7-9-24(20)25-17-27(40-10-12-41(5,13-11-40)19-46-47(43,44)45)38-18-26(25)39(4)28(42)29(2,3)21-14-22(30(32,33)34)16-23(15-21)31(35,36)37/h6-9,14-18H,10-13,19H2,1-5H3,(H-,43,44,45)

Molecular Formula

C31H35F6N4O5P

HBD / HBA

1 / 13

Liên kết có thể quay

8

Nguyên tử nặng

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.

Câu hỏi thường gặp

A prodrug of netupitant, a neurokinin-1 receptor antagonist used to prevent chemotherapy-induced nausea and vomiting, particularly delayed nausea. After intravenous administration, it is rapidly converted to netupitant which blocks substance P from triggering nausea signals in the brain. It is often combined with a 5-HT3 antagonist for broader antiemetic coverage.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Fosnetupitant 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). CHEMBL3989917. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 71544786. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

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.