Discovery and optimization of nonpeptide HIV-1 protease inhibitors
- 30 September 1996
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 4 (9) , 1401-1410
- https://doi.org/10.1016/0968-0896(96)00134-4
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- On the size of the active site in proteases. I. PapainPublished by Elsevier ,2005
- In vivo emergence of HIV-1 variants resistant to multiple protease inhibitorsNature, 1995
- Competitive Inhibition of HIV-1 Protease by Warfarin DerivativesBiochemical and Biophysical Research Communications, 1994
- Competitive Inhibition of HIV-1 Protease by 4-Hydroxy-benzopyran-2-ones and by 4-Hydroxy-6-phenylpyran-2-onesBiochemical and Biophysical Research Communications, 1994
- Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease InhibitorsScience, 1994
- STRUCTURE-BASED INHIBITORS OF HIV-1 PROTEASEAnnual Review of Biochemistry, 1993
- Using three-dimensional substructure searching to identify novel, non-peptidic inhibitors of HIV-1 proteaseTetrahedron Computer Methodology, 1990
- Design, Activity, and 2.8 Å Crystal Structure of a C 2 Symmetric Inhibitor Complexed to HIV-1 ProteaseScience, 1990
- Sub‐site preferences of the aspartic proteinase from the human immunodeficiency virus, HIV‐1FEBS Letters, 1990
- HIV-1 protease specificity of peptide cleavage is sufficient for processing of gag and pol polyproteinsBiochemical and Biophysical Research Communications, 1988