Thioamide Hydroxypyrothiones Supersede Amide Hydroxypyrothiones in Potency against Anthrax Lethal Factor

• Published in: Journal of medicinal chemistry 2009-02, Vol.52 (4), p.1063-1074
• Main Authors: Agrawal, Arpita, de Oliveira, César Augusto F, Cheng, Yuhui, Jacobsen, Jennifer A, McCammon, J. Andrew, Cohen, Seth M
• Format: Article
• Language: English
• Subjects: Amides - chemistry; Amides - pharmacology; Antigens, Bacterial; Bacterial Toxins - antagonists & inhibitors; Bacteriology; Biological and medical sciences; Catalytic Domain; Fundamental and applied biological sciences. Psychology; Hydrogen Bonding; Ligands; Medical sciences; Microbiology; Miscellaneous; Models, Molecular; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains; Pharmacology. Drug treatments; Protein Binding; Structure-Activity Relationship; Thioamides - chemistry; Thioamides - pharmacology; Thiones - chemistry; Thiones - pharmacology
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm8013212

Anthrax lethal factor (LF) is a critical virulence factor in the pathogenesis of anthrax. A structure−activity relationship (SAR) of potential lethal factor inhibitors (LFi) is presented in which the zinc-binding group (ZBG), linker, and backbone moieties for a series of hydroxypyrone-based compounds were systematically varied. It was found that hydroxypyrothione ZBGs generate more potent inhibitors than hydroxypyrone ZBGs. Furthermore, coupling the hydroxypyrothione to a backbone group via a thioamide bond improves potency when compared to an amide linker. QM/MM studies show that the thioamide bond in these inhibitors allows for the formation of two additional hydrogen bonds with the protein active site. In both types of hydroxypyrothione compounds, ligand efficiencies of 0.29−0.54 kcal mol−1 per heavy atom were achieved. The results highlight the need for a better understanding to optimize the interplay between the ZBG, linker, and backbone to get improved LFi.