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Human Immunodeficiency Virus Type 1 Protease Inhibitors: Evaluation of Resistance Engendered by Amino Acid Substitutions in the Enzyme's Substrate Binding Site
X-ray crystallographic structure of a complex between a synthetic protease of human immunodeficiency virus 1 and a substrate-based hydroxyethylamine inhibitor.
In vitro isolation and identification of human immunodeficiency virus (HIV) variants with reduced sensitivity to C-2 symmetrical inhibitors of HIV type 1 protease.
Studies of HIV-1 Protease Inhibitors. I. Incorporation of a Reduced Peptide, Simple Aminoalcohol, and Statine Analog at the Scissile Site of Substrate Sequences.
A Site‐Saturated Mutagenesis Study of Pentaerythritol Tetranitrate Reductase Reveals that Residues 181 and 184 Influence Ligand Binding, Stereochemistry and Reactivity
New imidazolidindionedioximes and their Pt(II) complexes: Synthesis and investigation of their antitumoral activities on breast cancer cells
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