Efavirenz
A non-nucleoside reverse transcriptase inhibitor used as part of combination antiretroviral therapy to treat HIV-1 infection. It blocks a viral enzyme essential for HIV to copy its genetic material.
Masse moléculaire
315,6700 g/mol
LogP
4,00
TPSA
38,30 Ų
Règle des 5 de Lipinski
Conforme
Aires thérapeutiques
Mécanisme d'action
Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.
Structure 2D
Cite this structure
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SMILES
O=C1Nc2ccc(Cl)cc2[C@@](C#CC2CC2)(C(F)(F)F)O1
InChI
InChI=1S/C14H9ClF3NO2/c15-9-3-4-11-10(7-9)13(14(16,17)18,21-12(20)19-11)6-5-8-1-2-8/h3-4,7-8H,1-2H2,(H,19,20)/t13-/m0/s1
Molecular Formula
C14H9ClF3NO2
HBD / HBA
1 / 5
Liaisons Rotatives
1
Atomes Lourds
21
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.
Foire aux questions
A non-nucleoside reverse transcriptase inhibitor used as part of combination antiretroviral therapy to treat HIV-1 infection. It blocks a viral enzyme essential for HIV to copy its genetic material.
Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.
Yes, Efavirenz 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). CHEMBL223228. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 64139. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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