Delavirdine Mesylate

CHEMBL929 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
552.7 g/mol
LogP
Phase
4

The mesylate salt form of delavirdine, a first-generation NNRTI used in combination antiretroviral regimens for HIV-1 infection. It requires multiple daily doses and has significant drug interactions due to CYP3A4 inhibition.

Peso Molecular

552,7000 g/mol

TPSA

182,00 Ų

Mecanismo de Ação

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

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

Estrutura 2D

SVG PNG

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SMILES

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

InChI

InChI=1S/C22H28N6O3S.CH4O3S/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;1-5(2,3)4/h4-8,13-15,24-26H,9-12H2,1-3H3;1H3,(H,2,3,4)

Molecular Formula

C23H32N6O6S2

HBD / HBA

4 / 10

Ligações Rotacionáveis

6

Átomos Pesados

37

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.

Perguntas frequentes

The mesylate salt form of delavirdine, a first-generation NNRTI used in combination antiretroviral regimens for HIV-1 infection. It requires multiple daily doses and has significant drug interactions due to CYP3A4 inhibition.

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

Yes, Delavirdine Mesylate 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). CHEMBL929. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 441386. Chemical information database.

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

Aviso Médico

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.