Substituted 1,6-naphthyridines as human cytomegalovirus inhibitors: conformational requirements.
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L. Chan | H. Jin | T. Stefanac | S. May | G. Falardeau | J. Lavallée
[1] L. Chan,et al. Discovery of 1,6-naphthyridines as a novel class of potent and selective human cytomegalovirus inhibitors. , 1999, Journal of medicinal chemistry.
[2] J M Morin,et al. Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs. , 1995, Journal of medicinal chemistry.
[3] J. Decerprit,et al. Synthesis and structure-activity relationships of new ACAT inhibitors , 1995 .