Grazoprevir Anhydrous

CHEMBL2063090 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
766.9 g/mol
LogP
4.7
Phase
4

An anhydrous form of grazoprevir, a hepatitis C virus NS3/4A protease inhibitor used in combination with other antivirals to treat chronic hepatitis C infection.

Peso Molecular

766,9000 g/mol

LogP

4,70

TPSA

204,00 Ų

Regra dos 5 de Lipinski

Reprovado

Mecanismo de Ação

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

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

Estrutura 2D

SVG PNG

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SMILES

C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H]2CN1C(=O)[C@H](C(C)(C)C)NC(=O)O[C@@H]1C[C@H]1CCCCCc1nc3ccc(OC)cc3nc1O2)C(=O)NS(=O)(=O)C1CC1

InChI

InChI=1S/C38H50N6O9S/c1-6-22-19-38(22,35(47)43-54(49,50)25-13-14-25)42-32(45)29-18-24-20-44(29)34(46)31(37(2,3)4)41-36(48)53-30-16-21(30)10-8-7-9-11-27-33(52-24)40-28-17-23(51-5)12-15-26(28)39-27/h6,12,15,17,21-22,24-25,29-31H,1,7-11,13-14,16,18-20H2,2-5H3,(H,41,48)(H,42,45)(H,43,47)/t21-,22-,24-,29+,30-,31-,38-/m1/s1

Molecular Formula

C38H50N6O9S

HBD / HBA

3 / 11

Ligações Rotacionáveis

8

Átomos Pesados

54

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.

Perguntas frequentes

An anhydrous form of grazoprevir, a hepatitis C virus NS3/4A protease inhibitor used in combination with other antivirals to treat chronic hepatitis C infection.

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

Yes, Grazoprevir Anhydrous 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). CHEMBL2063090. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 44603531. Chemical information database.

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

Aviso Médico

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.