Dolutegravir Sodium

CHEMBL1213165 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
441.4 g/mol
LogP
Phase
4

The sodium salt form of dolutegravir, used in some pharmaceutical preparations of this integrase inhibitor for HIV treatment. As the parent drug dolutegravir, it prevents HIV from inserting its genetic material into human cell DNA. This salt form may be used to optimize solubility and bioavailability in specific formulations.

Khối lượng phân tử

441,4000 g/mol

TPSA

102,00 Ų

Lĩnh vực điều trị

Cơ chế tác dụng

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

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

Cấu trúc 2D

SVG PNG

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SMILES

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

InChI

InChI=1S/C20H19F2N3O5.Na/c1-10-4-5-30-15-9-24-8-13(17(26)18(27)16(24)20(29)25(10)15)19(28)23-7-11-2-3-12(21)6-14(11)22;/h2-3,6,8,10,15,27H,4-5,7,9H2,1H3,(H,23,28);/q;+1/p-1/t10-,15+;/m1./s1

Molecular Formula

C20H18F2N3NaO5

HBD / HBA

1 / 8

Liên kết có thể quay

3

Nguyên tử nặng

31

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.

Câu hỏi thường gặp

The sodium salt form of dolutegravir, used in some pharmaceutical preparations of this integrase inhibitor for HIV treatment. As the parent drug dolutegravir, it prevents HIV from inserting its genetic material into human cell DNA. This salt form may be used to optimize solubility and bioavailability in specific formulations.

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

Yes, Dolutegravir 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). CHEMBL1213165. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 46216142. Chemical information database.

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

Tuyên bố miễn trách y tế

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.