Glecaprevir

CHEMBL3545363 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
838.9 g/mol
LogP
4.6
Phase
4

A NS3/4A protease inhibitor used as part of a combination antiviral regimen to treat chronic hepatitis C infection across all major genotypes. It works by blocking a viral enzyme essential for processing the hepatitis C polyprotein into functional components required for viral replication. When combined with pibrentasvir, it offers a highly effective pan-genotypic cure with a short treatment duration.

Molecular Weight

838.9000 g/mol

LogP

4.60

TPSA

204.00 Ų

Lipinski RO5

Fail

Therapeutic Areas

Mechanism of Action

Inhibits viral protease enzymes required for the cleavage of polyprotein precursors into functional viral proteins, blocking viral maturation and replication.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Inhibits viral protease enzymes required for the cleavage of polyprotein precursors into functional viral proteins, blocking viral maturation and replication.

2D Structure

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SMILES

CC(C)(C)[C@@H]1NC(=O)O[C@@H]2CCC[C@H]2OC/C=C/C(F)(F)c2nc3ccccc3nc2O[C@@H]2C[C@@H](C(=O)N[C@]3(C(=O)NS(=O)(=O)C4(C)CC4)C[C@H]3C(F)F)N(C2)C1=O

InChI

InChI=1S/C38H46F4N6O9S/c1-35(2,3)28-32(50)48-19-20(17-24(48)30(49)46-37(18-21(37)29(39)40)33(51)47-58(53,54)36(4)14-15-36)56-31-27(43-22-9-5-6-10-23(22)44-31)38(41,42)13-8-16-55-25-11-7-12-26(25)57-34(52)45-28/h5-6,8-10,13,20-21,24-26,28-29H,7,11-12,14-19H2,1-4H3,(H,45,52)(H,46,49)(H,47,51)/b13-8+/t20-,21+,24+,25-,26-,28-,37-/m1/s1

Molecular Formula

C38H46F4N6O9S

HBD / HBA

3 / 15

Rotatable Bonds

7

Heavy Atoms

58

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.

Frequently Asked Questions

A NS3/4A protease inhibitor used as part of a combination antiviral regimen to treat chronic hepatitis C infection across all major genotypes. It works by blocking a viral enzyme essential for processing the hepatitis C polyprotein into functional components required for viral replication. When combined with pibrentasvir, it offers a highly effective pan-genotypic cure with a short treatment duration.

Inhibits viral protease enzymes required for the cleavage of polyprotein precursors into functional viral proteins, blocking viral maturation and replication.

Yes, Glecaprevir 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). CHEMBL3545363. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 66828839. Chemical information database.

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

Medical Disclaimer

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.