Etravirine

CHEMBL308954 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
435.3 g/mol
LogP
4.5
Phase
4

This non-nucleoside reverse transcriptase inhibitor blocks the HIV enzyme needed to convert its RNA into DNA inside human cells. It is used as part of combination therapy for treatment-experienced patients with HIV.

Berat Molekul

435,3000 g/mol

LogP

4,50

TPSA

121,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.

Struktur 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

Cc1cc(C#N)cc(C)c1Oc1nc(Nc2ccc(C#N)cc2)nc(N)c1Br

InChI

InChI=1S/C20H15BrN6O/c1-11-7-14(10-23)8-12(2)17(11)28-19-16(21)18(24)26-20(27-19)25-15-5-3-13(9-22)4-6-15/h3-8H,1-2H3,(H3,24,25,26,27)

Molecular Formula

C20H15BrN6O

HBD / HBA

2 / 7

Ikatan yang Dapat Dirotasi

4

Atom Berat

28

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.

Pertanyaan yang Sering Diajukan

This non-nucleoside reverse transcriptase inhibitor blocks the HIV enzyme needed to convert its RNA into DNA inside human cells. It is used as part of combination therapy for treatment-experienced patients with HIV.

Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.

Yes, Etravirine 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). CHEMBL308954. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 193962. Chemical information database.

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

Penyangkalan Medis

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.