Cabotegravir Sodium

CHEMBL3137330 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
427.3 g/mol
LogP
Phase
4

The sodium salt form of cabotegravir, used in injectable long-acting formulations for HIV treatment and prevention. It is administered intramuscularly and provides sustained drug levels over weeks to months. This formulation offers a major improvement in treatment convenience for people living with HIV.

Molekularmasse

427,3000 g/mol

TPSA

102,00 Ų

Therapeutische Bereiche

Wirkmechanismus

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

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

2D-Struktur

SVG PNG

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SMILES

C[C@H]1CO[C@@H]2Cn3cc(C(=O)NCc4ccc(F)cc4F)c(=O)c([O-])c3C(=O)N12.[Na+]

InChI

InChI=1S/C19H17F2N3O5.Na/c1-9-8-29-14-7-23-6-12(16(25)17(26)15(23)19(28)24(9)14)18(27)22-5-10-2-3-11(20)4-13(10)21;/h2-4,6,9,14,26H,5,7-8H2,1H3,(H,22,27);/q;+1/p-1/t9-,14+;/m0./s1

Molecular Formula

C19H16F2N3NaO5

HBD / HBA

1 / 8

Rotierbare Bindungen

3

Schwere Atome

30

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.

Häufig gestellte Fragen

The sodium salt form of cabotegravir, used in injectable long-acting formulations for HIV treatment and prevention. It is administered intramuscularly and provides sustained drug levels over weeks to months. This formulation offers a major improvement in treatment convenience for people living with HIV.

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

Yes, Cabotegravir 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). CHEMBL3137330. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 46215800. Chemical information database.

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

Medizinischer Haftungsausschluss

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.