Bictegravir Sodium

CHEMBL3989867 Phase 4 承認済み 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.

分子量

471.4000 g/mol

TPSA

102.00 Ų

治療領域

作用機序

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

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

2D構造

SVG PNG

Cite this structure


                        

Embed this structure


                        

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

回転可能結合数

3

重原子数

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.

よくある質問

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.

医学的免責事項

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.