Rilpivirine Hydrochloride

CHEMBL1628504 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
402.9 g/mol
LogP
Phase
4

The hydrochloride salt formulation of rilpivirine used to treat HIV-1 infection by blocking the reverse transcriptase enzyme the virus needs to replicate. It is often combined with other antiretroviral agents in single-tablet regimens for convenient once-daily dosing.

Berat Molekul

402,9000 g/mol

TPSA

97,40 Ų

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=C/C#N)cc(C)c1Nc1ccnc(Nc2ccc(C#N)cc2)n1.Cl

InChI

InChI=1S/C22H18N6.ClH/c1-15-12-18(4-3-10-23)13-16(2)21(15)27-20-9-11-25-22(28-20)26-19-7-5-17(14-24)6-8-19;/h3-9,11-13H,1-2H3,(H2,25,26,27,28);1H/b4-3+;

Molecular Formula

C22H19ClN6

HBD / HBA

3 / 6

Ikatan yang Dapat Dirotasi

5

Atom Berat

29

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

The hydrochloride salt formulation of rilpivirine used to treat HIV-1 infection by blocking the reverse transcriptase enzyme the virus needs to replicate. It is often combined with other antiretroviral agents in single-tablet regimens for convenient once-daily dosing.

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

Yes, Rilpivirine Hydrochloride 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). CHEMBL1628504. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 11711114. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

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.