Delavirdine

CHEMBL593 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
456.6 g/mol
LogP
2.4
Phase
4

A non-nucleoside reverse transcriptase inhibitor (NNRTI) that blocks HIV replication by binding to and inhibiting reverse transcriptase, used as part of combination antiretroviral therapy. It has been largely replaced by more potent and better-tolerated NNRTIs.

Molecular Weight

456.6000 g/mol

LogP

2.40

TPSA

119.00 Ų

Lipinski RO5

Pass

Mechanism of 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)

Mechanism

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

2D Structure

SVG PNG

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SMILES

CC(C)Nc1cccnc1N1CCN(C(=O)c2cc3cc(NS(C)(=O)=O)ccc3[nH]2)CC1

InChI

InChI=1S/C22H28N6O3S/c1-15(2)24-19-5-4-8-23-21(19)27-9-11-28(12-10-27)22(29)20-14-16-13-17(26-32(3,30)31)6-7-18(16)25-20/h4-8,13-15,24-26H,9-12H2,1-3H3

Molecular Formula

C22H28N6O3S

HBD / HBA

3 / 7

Rotatable Bonds

6

Heavy Atoms

32

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.

Frequently Asked Questions

A non-nucleoside reverse transcriptase inhibitor (NNRTI) that blocks HIV replication by binding to and inhibiting reverse transcriptase, used as part of combination antiretroviral therapy. It has been largely replaced by more potent and better-tolerated NNRTIs.

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

Yes, Delavirdine 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). CHEMBL593. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5625. Chemical information database.

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

Medical Disclaimer

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.