| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1365708 | Bioorganic & Medicinal Chemistry Letters | 2007 | 6 Pages | 
Abstract
												A novel class of sulfoximine-based pseudosymmetric HIV-1 protease inhibitors were designed and synthesized. The most active isomer (2S,2â²S) displays potent activity against HIV-1 protease as well as virus.
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											Authors
												Ding Lu, Robert Vince, 
											