
Bioorganic and Medicinal Chemistry Letters p. 3137 - 3142 (1999)
Update date:2022-08-05
Topics:
Smith, David G.
Gribble, Andrew D.
Haigh, David
Ife, Robert J.
Lavery, Patrick
Skett, Peter
Slingsby, Brian P.
Stacey, Rachel
Ward, Robert W.
West, Andrew
Aryl hydroxylamine derivatives have been synthesised that are some of the most potent inhibitors of hCMV protease prepared to date (IC50 14-60 nM). Mass spectrometry studies indicate that oxazinone derived hydroxylamines inhibit the enzyme by a
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