Mechanism of Action of the Ribopyranoside Benzimidazole GW275175X against Human Cytomegalovirus

Author:

Underwood Mark R.1,Ferris Robert G.2,Selleseth Dean W.2,Davis Michelle G.1,Drach John C.3,Townsend Leroy B.4,Biron Karen K.1,Boyd F. Leslie5

Affiliation:

1. Departments of International Clinical Virology

2. Virology

3. Department of Biologic and Materials Sciences, School of Dentistry

4. Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan 48109

5. Medicinal Chemistry, GlaxoSmithKline, Research Triangle Park, North Carolina 27709

Abstract

ABSTRACT New human cytomegalovirus (HCMV) therapies with novel mechanisms of action are needed to treat drug-resistant HCMV that arises during therapy with currently approved agents. 2-Bromo-5,6-dichloro-1-β- d -ribofuranosyl-1 H -benzimidazole (BDCRB) is an effective anti-HCMV agent with a novel mechanism of action, but problems with in vivo stability preclude clinical development. A d -ribopyranosyl derivative of BDCRB, GW275175X, displays similar antiviral activity without the in vivo stability problems. We present an initial description of the activity of GW275175X against HCMV, other herpesviruses, and selected nonherpesviruses. In addition, we show that it acts as a DNA maturation inhibitor like the parent compound, BDCRB, rather than via the mechanisms of action of 1263W94 or any anti-HCMV drugs approved for marketing. GW275175X is a promising candidate for clinical development as an anti-HCMV agent.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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