Bictegravir Sodium

CHEMBL3989867 Phase 4 Одобрено 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.

Молекулярная масса

471,4000 g/mol

TPSA

102,00 Ų

Терапевтические области

Механизм действия

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Механизм

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

2D Структура

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

Вращаемые Связи

3

Тяжёлые Атомы

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.

Часто задаваемые вопросы

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.

Медицинский отказ от ответственности

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.