Rajakulendran, Joy E.Oluwabusola, Emmanuel TopeCerone, MichelaSmith, Terry K.Adebisi, Olusoji O.Adedotun, AdefolaluPreet, GaganSoldatou, SylviaDeng, HaiEbel, RainerJaspars, Marcel2025-10-302025-07-04Rajakulendran, J E, Oluwabusola, E T, Cerone, M, Smith, T K, Adebisi, O O, Adedotun, A, Preet, G, Soldatou, S, Deng, H, Ebel, R & Jaspars, M 2025, 'N-Salicyl-amino acid derivatives with antiparasitic activity from Pseudomonas sp. UIAU-6B', Beilstein journal of organic chemistry, vol. 21, pp. 1388-1396. https://doi.org/10.3762/bjoc.21.1031860-5397https://hdl.handle.net/2164/26330We thank Russell Gray of the Marine Biodiscovery Centre, Aberdeen for assisting in NMR spectroscopy. Additionally, we are grateful to Blessing Akinboyo and Dr. Soji Fakoya of Ondo State University of Science and Technology in Okitipupa, Nigeria, for their assistance with the sediment collection. The graphics of pathogens depicted in the graphical abstract were designed using the Scratch software (Scratch is a project of the Scratch Foundation, in collaboration with the Lifelong Kindergarten Group at the MIT Media Lab). It is available for free at https://scratch.mit.edu, and are distributed under the terms of the Creative Commons Attribution-Share Alike 2.0 License, https://creativecommons.org/licenses/by-sa/2.0/. This content is not subject to CC BY 4.0.9325944engantiparasitic activitybiosynthesis pathwayphenolic siderophoresPseudomonas speciespseudomonineOrganic ChemistrySupplementary DataDASJournal article10.3762/bjoc.21.103http://www.scopus.com/inward/record.url?scp=105011868274&partnerID=8YFLogxK