Darunavir

CHEMBL1323 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
547.7 g/mol
LogP
2.9
Phase
4

A second-generation HIV protease inhibitor that prevents viral replication by blocking the enzyme that cleaves HIV polyproteins into functional components, always used boosted with cobicistat or ritonavir. It has a high barrier to resistance and remains active against many PI-resistant viral strains.

分子量

547.7000 g/mol

LogP

2.90

TPSA

149.00 Ų

Lipinski 五规则

符合

治疗领域

作用机制

Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.

二维结构

SVG PNG

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SMILES

CC(C)CN(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc(N)cc1

InChI

InChI=1S/C27H37N3O7S/c1-18(2)15-30(38(33,34)21-10-8-20(28)9-11-21)16-24(31)23(14-19-6-4-3-5-7-19)29-27(32)37-25-17-36-26-22(25)12-13-35-26/h3-11,18,22-26,31H,12-17,28H2,1-2H3,(H,29,32)/t22-,23-,24+,25-,26+/m0/s1

Molecular Formula

C27H37N3O7S

HBD / HBA

3 / 9

可旋转键数

12

重原子数

38

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.

常见问题

A second-generation HIV protease inhibitor that prevents viral replication by blocking the enzyme that cleaves HIV polyproteins into functional components, always used boosted with cobicistat or ritonavir. It has a high barrier to resistance and remains active against many PI-resistant viral strains.

Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.

Yes, Darunavir 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). CHEMBL1323. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 213039. Chemical information database.

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

医疗免责声明

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.