Fosamprenavir Calcium

CHEMBL1200734 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
623.7 g/mol
LogP
Phase
4

This calcium salt prodrug form is converted by enzymes in the intestinal wall to amprenavir, which then inhibits the HIV protease enzyme to prevent viral replication. It is used in combination with other antiretrovirals to treat HIV/AIDS and offers improved absorption compared to the parent drug.

Masse moléculaire

623,7000 g/mol

TPSA

192,00 Ų

Aires thérapeutiques

Mécanisme d'action

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Structure 2D

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SMILES

CC(C)CN(C[C@@H](OP(=O)([O-])[O-])[C@H](Cc1ccccc1)NC(=O)O[C@H]1CCOC1)S(=O)(=O)c1ccc(N)cc1.[Ca+2]

InChI

InChI=1S/C25H36N3O9PS.Ca/c1-18(2)15-28(39(33,34)22-10-8-20(26)9-11-22)16-24(37-38(30,31)32)23(14-19-6-4-3-5-7-19)27-25(29)36-21-12-13-35-17-21;/h3-11,18,21,23-24H,12-17,26H2,1-2H3,(H,27,29)(H2,30,31,32);/q;+2/p-2/t21-,23-,24+;/m0./s1

Molecular Formula

C25H34CaN3O9PS

HBD / HBA

2 / 11

Liaisons Rotatives

13

Atomes Lourds

40

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 calcium salt prodrug form is converted by enzymes in the intestinal wall to amprenavir, which then inhibits the HIV protease enzyme to prevent viral replication. It is used in combination with other antiretrovirals to treat HIV/AIDS and offers improved absorption compared to the parent drug.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Fosamprenavir Calcium 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). CHEMBL1200734. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 131535. Chemical information database.

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

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.