Nevirapine
This non-nucleoside reverse transcriptase inhibitor is used as part of combination antiretroviral therapy to treat HIV infection in adults and children. It works by directly blocking the HIV enzyme needed to copy the virus's genetic material, reducing the viral load in the body.
Khối lượng phân tử
266,3000 g/mol
LogP
2,00
TPSA
58,10 Ų
Lipinski RO5
Đạt
Lĩnh vực điều trị
Cơ chế tác dụng
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.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
Cc1ccnc2c1NC(=O)c1cccnc1N2C1CC1
InChI
InChI=1S/C15H14N4O/c1-9-6-8-17-14-12(9)18-15(20)11-3-2-7-16-13(11)19(14)10-4-5-10/h2-3,6-8,10H,4-5H2,1H3,(H,18,20)
Molecular Formula
C15H14N4O
HBD / HBA
1 / 4
Liên kết có thể quay
1
Nguyên tử nặng
20
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.
Câu hỏi thường gặp
This non-nucleoside reverse transcriptase inhibitor is used as part of combination antiretroviral therapy to treat HIV infection in adults and children. It works by directly blocking the HIV enzyme needed to copy the virus's genetic material, reducing the viral load in the body.
Inhibits viral reverse transcriptase, blocking the conversion of viral RNA to DNA and preventing viral replication in infected host cells.
Yes, Nevirapine 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). CHEMBL57. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 4463. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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