Methyl propiolate and 3-butynone: starting points for synthesis of amphiphilic 1,2,3-triazole peptidomimetics for antimicrobial evaluation

• Published in: Bioorganic & Medicinal Chemistry
• Main Authors: Bakka, Thomas Aleksander, Strøm, Morten B., Andersen, Jeanette Hammer, Gautun, Odd Reidar
• Format: Article in Journal/Newspaper
• Language: English
• Published: Elsevier 2017
• Subjects: VDP::Matematikk og Naturvitenskap: 400::Kjemi: 440::Organisk kjemi: 441; VDP::Mathematics and natural science: 400::Chemistry: 440::Organic chemistry: 441; Arctic
• Online Access: https://hdl.handle.net/10037/11419; https://doi.org/10.1016/j.bmc.2017.07.060

Accepted manuscript version. Published version available at https://doi.org/10.1016/j.bmc.2017.07.060 A library of 29 small 1,4-substituted 1,2,3-triazoles was prepared for studies of antimicrobial activity. The pharmacophore model investigated with these substrates was based on small peptidomimetics of antimicrobial peptides and antimicrobials isolated from marine organisms from sub-arctic regions. Using methyl 1,2,3-triazole-carboxylates and 1,2,3-triazole methyl ketones prepared through “click” chemistry we were able to synthesize the different cationic amphiphiles through three steps or less. Several structural modifications to the lipopohilic side and hydrophilic sides of the amphiphiles were investigated and compared with regards to antimicrobial activity and cytotoxicity in particular. The most promising amphiphile 10f displayed minimum inhibitory concentrations (MICs) between 4 - 16 µg/mL against Gram-positive Enterococcus faecalis, Staphylococcus aureus, Streptococcus agalacticae, and Gram-negative Escherichia coli and Pseudomonas aeruginosa. The decent level of antimicrobial activity and biofilm inhibition, short synthesis, and accessible reagents, makes this type of amphiphilic mimics interesting leads for further development.