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.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ding Lu, Robert Vince,