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Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas
Brent R Stranix1, Gilles Sauvé, Abderrahim Bouzide
1Procyon Biopharma Inc., 1650 Trans-Canada Highway, Suite 200, Dorval, Quebec, Canada, H9P 1H7. bstranix@procyonbiopharma.com
Abstract:
A series of lysine sulfonamide analogues bearing a Nepsilon-benzylic ureas was synthesized using both solution-phase and solid-phase approaches. A novel synthetic route of Nalpha-(alkyl)-Nalpha-(sulfonamides)lysinol using alpha-amino-caprolactam was developed. Evaluation of these novel protease inhibitors revealed compounds with high potency against wild-type HIV virus.
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