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Nucleoside analogues as highly potent and selective inhibitors of herpes simplex virus thymidine kinase
J A Martin1, R W Lambert, J H Merrett
1Department of Medicinal Chemistry, Roche Discovery Welwyn, Broadwater Road, Welwyn Garden City, AL7 3AY, Herts, UK. joseph.martin@roche.com
Abstract:
A series of carboxamide derivatives of 5'-amino-2',5'-dideoxy-5-ethyluridine has been prepared as inhibitors of HSV-TK (herpes simplex virus thymidine kinase). The most potent compounds were derived from xanthene, thioxanthene and dihydroanthracene carboxylic acids. The lead compounds show subnanomolar IC(50) values against HSV TKs.
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