Doravirine

CHEMBL2364608 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
425.7 g/mol
LogP
2.1
Phase
4

A non-nucleoside reverse transcriptase inhibitor used to treat HIV-1 infection as part of a combination antiretroviral regimen. It blocks a key enzyme the virus needs to copy its genetic material.

Khối lượng phân tử

425,7000 g/mol

LogP

2,10

TPSA

98,00 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)

Cơ chế

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

Cấu trúc 2D

SVG PNG

Cite this structure


                        

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SMILES

Cn1c(Cn2ccc(C(F)(F)F)c(Oc3cc(Cl)cc(C#N)c3)c2=O)n[nH]c1=O

InChI

InChI=1S/C17H11ClF3N5O3/c1-25-13(23-24-16(25)28)8-26-3-2-12(17(19,20)21)14(15(26)27)29-11-5-9(7-22)4-10(18)6-11/h2-6H,8H2,1H3,(H,24,28)

Molecular Formula

C17H11ClF3N5O3

HBD / HBA

1 / 8

Liên kết có thể quay

4

Nguyên tử nặng

29

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

A non-nucleoside reverse transcriptase inhibitor used to treat HIV-1 infection as part of a combination antiretroviral regimen. It blocks a key enzyme the virus needs 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, Doravirine 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). CHEMBL2364608. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 58460047. Chemical information database.

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

Tuyên bố miễn trách y tế

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.