Keywords

ChemistryDipeptideAmideCathepsin SCathepsinStereochemistryPeptide bondSelectivityEnzyme inhibitorCarboxamideChemical synthesisCathepsin KNitrogen atomHydrogen bondCathepsin BPeptideEnzymeBiochemistryIn vitroOrganic chemistryMoleculeGroup (periodic table)Catalysis

Affiliated Institutions

Related Publications

Asymmetric Synthesis of Chiral Organofluorine Compounds:  Use of Nonracemic Fluoroiodoacetic Acid as a Practical Electrophile and Its Application to the Synthesis of Monofluoro Hydroxyethylene Dipeptide Isosteres within a Novel Series of HIV Protease Inhibitors

Two stereoselective routes to a series of diastereomeric inhibitors of HIV protease, monofluorinated analogues of the Merck HIV protease inhibitor indinavir, are described. The ...

2001 Journal of the American Chemical Society 140 citations

Publication Info

Year
2005
Type
article
Volume
15
Issue
21
Pages
4741-4744
Citations
135
Access
Closed

External Links

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

135
OpenAlex

Cite This

W. Cameron Black, Christopher I. Bayly, Dana Davis et al. (2005). Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K. Bioorganic & Medicinal Chemistry Letters , 15 (21) , 4741-4744. https://doi.org/10.1016/j.bmcl.2005.07.071

Identifiers

DOI
10.1016/j.bmcl.2005.07.071