Bictegravir Sodium
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)
Inhibits viral integrase, preventing the insertion of viral DNA into the host cell genome and blocking viral replication.
2D構造
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
- 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.
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