Delavirdine Mesylate
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.
Moleküler Ağırlık
552,7000 g/mol
TPSA
182,00 Ų
Etki Mekanizması
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.
2D Yapı
Cite this structure
Embed this structure
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
Döndürülebilir Bağlar
6
Ağır Atomlar
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.
Sıkça Sorulan Sorular
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
- 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.
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