Simeprevir

CHEMBL501849 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
749.9 g/mol
LogP
4.8
Phase
4

Simeprevir is a macrocyclic peptidomimetic inhibitor of the hepatitis C virus NS3/4A serine protease, used for the treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infection in combination with other antiviral agents. By competitively binding the NS3/4A protease active site, it blocks viral polyprotein processing and inhibits HCV replication. It achieves high sustained virologic response rates when combined with sofosbuvir or pegylated interferon plus ribavirin.

분자량

749.9000 g/mol

LogP

4.80

TPSA

194.00 Ų

리핀스키 5의 법칙

통과

치료 영역

작용 기전

Inhibits the NS3/4A serine protease of hepatitis C virus, blocking the processing of the viral polyprotein essential for replication.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

기전

Inhibits the NS3/4A serine protease of hepatitis C virus, blocking the processing of the viral polyprotein essential for replication.

2D 구조

SVG PNG

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SMILES

COc1ccc2c(O[C@@H]3C[C@H]4C(=O)N[C@]5(C(=O)NS(=O)(=O)C6CC6)C[C@H]5/C=C\CCCCN(C)C(=O)[C@@H]4C3)cc(-c3nc(C(C)C)cs3)nc2c1C

InChI

InChI=1S/C38H47N5O7S2/c1-21(2)30-20-51-35(40-30)29-18-32(26-13-14-31(49-5)22(3)33(26)39-29)50-24-16-27-28(17-24)36(45)43(4)15-9-7-6-8-10-23-19-38(23,41-34(27)44)37(46)42-52(47,48)25-11-12-25/h8,10,13-14,18,20-21,23-25,27-28H,6-7,9,11-12,15-17,19H2,1-5H3,(H,41,44)(H,42,46)/b10-8-/t23-,24-,27-,28-,38-/m1/s1

Molecular Formula

C38H47N5O7S2

HBD / HBA

2 / 10

회전 가능 결합

8

무거운 원자

52

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.

자주 묻는 질문

Simeprevir is a macrocyclic peptidomimetic inhibitor of the hepatitis C virus NS3/4A serine protease, used for the treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infection in combination with other antiviral agents. By competitively binding the NS3/4A protease active site, it blocks viral polyprotein processing and inhibits HCV replication. It achieves high sustained virologic response rates when combined with sofosbuvir or pegylated interferon plus ribavirin.

Inhibits the NS3/4A serine protease of hepatitis C virus, blocking the processing of the viral polyprotein essential for replication.

Yes, Simeprevir 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). CHEMBL501849. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 24873435. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

의학적 면책조항

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.