Drug intelligence / Profile preview

eprociclovir

Development stage
Discontinued
Lead developer
Ajinomoto
Modality
Small Molecules
Administration
Ophthalmic
01

Overview

Eprociclovir is a **small molecule nucleoside analogue antiviral** and an acyclovir analogue developed by **Ajinomoto**. It is phosphorylated in virus-infected cells by viral and cellular enzymes, including viral thymidine kinase, to an active triphosphate metabolite that inhibits **viral DNA-directed DNA polymerase**, thereby suppressing replication of herpesviruses. Preclinical reports describe activity against multiple human herpesviruses including **herpes simplex virus** and **cytomegalovirus**, with development explored particularly for **herpetic keratitis** using an ophthalmic eyedrop formulation. Available information indicates that development was **discontinued**, and animal studies have reported **nephrotoxicity**.

Other names
eprociclovir
02

Targets

Herpesvirus DNA polymeraseHSV-TK (Herpes simplex virus type 1 thymidine kinase (HSV1-TK))

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