Synthesis and methemoglobinemia-inducing properties of benzocaine isosteres designed as humane rodenticides.

Abstract

A number of isosteres (oxadiazoles, thiadiazoles, tetrazoles and diazines) of benzocaine were prepared and evaluated for their capacity to induce methemoglobinemia-with a view to their possible application as humane pest control agents. It was found that an optimal lipophilicity for the formation of methemoglobin (metHb) in vitro existed within each series, with 1,2,4-oxadiazole 3 (metHb%=61.0±3.6) and 1,3,4-oxadiazole 10 (metHb%=52.4±0.9) demonstrating the greatest activity. Of the 5 candidates (compounds 3, 10, 11, 13 and 23) evaluated in vivo, failure to induce a lethal end-point at doses of 120mg/kg was observed in all cases. Inadequate metabolic stability, particularly towards hepatic enzymes such as the CYPs, was postulated as one reason for their failure.

• Authors: Daniel Conole, Thorsten M Beck, Morgan Jay-Smith, Malcolm D Tingle, Charles T Eason, Margaret A Brimble, David Rennison
• Journal: Bioorganic & medicinal chemistry (Bioorg Med Chem) Vol. 22 Issue 7 Pg. 2220-35 (Apr 01 2014) ISSN: 1464-3391 [Electronic] England
• PMID: 24602400 (Publication Type: Journal Article)
• Copyright: Copyright © 2014 Elsevier Ltd. All rights reserved.

Chemical References

• Oxadiazoles
• Rodenticides
• Methemoglobin
• Benzocaine

Topics

• Animals
• Benzocaine (chemical synthesis, chemistry, pharmacology)
• Drug Design
• Female
• Male
• Methemoglobin (biosynthesis)
• Methemoglobinemia (metabolism)
• Molecular Structure
• Oxadiazoles (chemical synthesis, chemistry, pharmacology)
• Rats
• Rats, Sprague-Dawley
• Rats, Wistar
• Rodenticides (chemical synthesis, chemistry, pharmacology)