Glecaprevir

CHEMBL3545363 Phase 4 Zugelassen 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.

Molekularmasse

838,9000 g/mol

LogP

4,60

TPSA

204,00 Ų

Lipinski-Regel der Fünf

Nicht bestanden

Therapeutische Bereiche

Wirkmechanismus

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

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

2D-Struktur

SVG PNG

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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

Rotierbare Bindungen

7

Schwere Atome

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.

Häufig gestellte Fragen

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.

Medizinischer Haftungsausschluss

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.