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Synthesis and evaluation of fluorogenic 2-amino-1,8-naphthyridine derivatives for the detection of bacteria

journal contribution
posted on 2024-11-01, 10:14 authored by Linda Varadi, Mark Gray, Paul Groundwater, Andrew Hall, Arthur James, Sylvain Orenga, John Perry, Rosaleen Anderson
Several novel fluorogenic N-aminoacylnaphthyridine substrates were synthesized in good yield and tested for their ability to detect pathogenic bacteria in agar-based cell culture. Simple 2-N-(beta-alanyl)amino-5,7-dialkylnaphthyridine substrates were selectively hydrolysed by beta-alanylaminopeptidase expressing bacteria, but were subject to diffusion in the agar medium. Diffusion was reduced in the 2-N-(beta-alanyl)amino-7-alkylnaphthyridine substrates with longer alkyl chains, but inhibition of growth was increased. 2-N-(beta-Alanyl)amino-7-octylnaphthyridine inhibited the growth of all species tested, except for strains resistant to colistin/polymyxin, providing a rationale for the development of substrates for the selective detection of drug resistant species in clinical samples.

History

Journal

Organic and Biomolecular Chemistry

Volume

10

Issue

13

Start page

2578

End page

2589

Total pages

12

Publisher

Royal Society of Chemistry

Place published

United Kingdom

Language

English

Copyright

This journal is © The Royal Society of Chemistry 2012

Former Identifier

2006092830

Esploro creation date

2020-06-22

Fedora creation date

2019-07-18

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