A review on HCV inhibitors: Significance of non-structural polyproteins

Narayana Murthy Ganta1, Gangaraju Gedda2, Bethi Rathnakar3

  • 1Department of Pharmaceutical Chemistry, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Medak, Telangana, 502313, India.

Insights

Hepatitis C virus (HCV) infection affects millions globally, causing severe liver disease. This review focuses on NS5B protein inhibitors as potential new drug candidates for treating HCV.

Area of Science:

  • Medicinal Chemistry
  • Hepatology
  • Virology

Background:

  • Hepatitis C virus (HCV) infection is a major global health issue, leading to significant morbidity and mortality.
  • Chronic HCV infection affects 130-150 million individuals worldwide, causing liver damage like cirrhosis and hepatocellular carcinoma.
  • HCV NS5B protein is a key therapeutic target for developing new antiviral drugs.

Purpose of the Study:

  • To review research on Hepatitis C virus NS5B protein inhibitors.
  • To concentrate on hit identification, lead optimization, ADME evaluation, and SAR data for anti-HCV compounds.
  • To provide a resource for medicinal chemists developing novel HCV therapeutics.

Main Methods:

  • Literature review of published research on NS5B inhibitors and other functional inhibitors.
  • Analysis of hit investigation and hit-to-lead optimization strategies.
  • Evaluation of ADME parameters and Structure-Activity Relationship (SAR) data for identified compounds.

Main Results:

  • Several preclinical drug molecules targeting NS5B have emerged.
  • The review details SAR and ADME data for various compound classes.
  • Compound activity against NS5B and other relevant targets is discussed.

Conclusions:

  • NS5B inhibitors represent a promising avenue for Hepatitis C virus treatment.
  • This review offers valuable insights into the development of effective anti-HCV agents.
  • Medicinal chemists can utilize this information to advance HCV drug discovery programs.

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