Bictegravir Sodium

CHEMBL3989867 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
471.4 g/mol
LogP
Phase
4

The sodium salt form of bictegravir, an HIV integrase inhibitor used in combination antiretroviral therapy for HIV-1 infection. It is part of a once-daily fixed-dose combination that also includes two other antiretroviral agents. It has a high barrier to resistance development.

Masse moléculaire

471,4000 g/mol

TPSA

102,00 Ų

Aires thérapeutiques

Mécanisme d'action

Inhibits viral integrase, preventing the insertion of viral DNA into the host cell genome and blocking viral replication.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Inhibits viral integrase, preventing the insertion of viral DNA into the host cell genome and blocking viral replication.

Structure 2D

SVG PNG

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SMILES

O=C(NCc1c(F)cc(F)cc1F)c1cn2c(c([O-])c1=O)C(=O)N1[C@H]3CC[C@H](C3)O[C@@H]1C2.[Na+]

InChI

InChI=1S/C21H18F3N3O5.Na/c22-9-3-14(23)12(15(24)4-9)6-25-20(30)13-7-26-8-16-27(10-1-2-11(5-10)32-16)21(31)17(26)19(29)18(13)28;/h3-4,7,10-11,16,29H,1-2,5-6,8H2,(H,25,30);/q;+1/p-1/t10-,11+,16+;/m0./s1

Molecular Formula

C21H17F3N3NaO5

HBD / HBA

1 / 9

Liaisons Rotatives

3

Atomes Lourds

33

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

The sodium salt form of bictegravir, an HIV integrase inhibitor used in combination antiretroviral therapy for HIV-1 infection. It is part of a once-daily fixed-dose combination that also includes two other antiretroviral agents. It has a high barrier to resistance development.

Inhibits viral integrase, preventing the insertion of viral DNA into the host cell genome and blocking viral replication.

Yes, Bictegravir Sodium 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). CHEMBL3989867. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 102593990. 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.