Identification and isolation of insecticidal oxazoles from Pseudomonas spp.

Scholarly Works

• Liu, J.-R.; Jiang, E.-Y.; Sukhbaatar, O.; Zhang, W.-H.; Zhang, M.-Z.; Yang, G.-F.; Gu, Y.-C. Natural and synthetic 5-(3'-indolyl)oxazoles: Biological activity, chemical synthesis and advanced molecules. Medicinal research reviews 2024. doi:10.1002/med.22078
• Sekar, P.; Gupta, A.; English, L. E.; Rabbitt, C. E.; Male, L.; Jupp, A. R.; Davies, P. W. Regiodivergent Synthesis of 4- and 5-Sulfenyl Oxazoles from Alkynyl Thioethers. Chemistry (Weinheim an der Bergstrasse, Germany) 2024, 30, e202401465. doi:10.1002/chem.202401465
• Park, J.; Mahida, N.; Ho, G.; Pena, E.; Makabenta, J. M. V.; Aneke, S.; Jiang, M.; Bouthillette, L. M.; Holz, S. E.; Hassan, M. A.; Wolfe, A. L.; Rotello, V. M. Integration of Antimicrobials and Delivery Systems: Synergistic Antibiofilm Activity with Biodegradable Nanoemulsions Incorporating Pseudopyronine Analogs. Antibiotics (Basel, Switzerland) 2023, 12, 1240. doi:10.3390/antibiotics12081240
• Joshi, S.; Mehra, M.; Singh, R.; Kakar, S. Review on Chemistry of Oxazole derivatives: Current to Future Therapeutic Prospective. Egyptian Journal of Basic and Applied Sciences 2023, 10, 218–239. doi:10.1080/2314808x.2023.2171578
• Liu, X.; Wang, Y.; Zaleta-Pinet, D. A.; Borris, R. P.; Clark, B. R. Antibacterial and Anti-Biofilm Activity of Pyrones from a Pseudomonas mosselii Strain. Antibiotics (Basel, Switzerland) 2022, 11, 1655. doi:10.3390/antibiotics11111655
• Mao, Z.; Zeng, H. Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles. RSC advances 2022, 12, 24857–24860. doi:10.1039/d2ra04559a
• Zhang, S.; Zhang, L.; Zhu, J.; Hong, C.; Chen, Z.; Si, T.; Liu, T. Genomic and Metabolomic Investigation of a Rhizosphere Isolate Streptomyces netropsis WLXQSS-4 Associated with a Traditional Chinese Medicine. Molecules (Basel, Switzerland) 2021, 26, 2147. doi:10.3390/molecules26082147
• Brachmann, A. O.; Probst, S. I.; Rüthi, J.; Dudko, D.; Bode, H. B.; Piel, J. A Desaturase‐Like Enzyme Catalyzes Oxazole Formation in Pseudomonas Indolyloxazole Alkaloids. Angewandte Chemie (International ed. in English) 2021, 60, 8781–8785. doi:10.1002/anie.202014491
• Brachmann, A. O.; Probst, S. I.; Rüthi, J.; Dudko, D.; Bode, H. B.; Piel, J. A Desaturase‐Like Enzyme Catalyzes Oxazole Formation in Pseudomonas Indolyloxazole Alkaloids. Angewandte Chemie 2021, 133, 8863–8867. doi:10.1002/ange.202014491
• Kretsch, A. M.; Morgan, G. L.; Acken, K. A.; Barr, S. A.; Li, B. Pseudomonas Virulence Factor Pathway Synthesizes Autoinducers That Regulate the Secretome of a Pathogen. ACS chemical biology 2021, 16, 501–509. doi:10.1021/acschembio.0c00901
• Jeffries, K. A.; Farrell, E. K.; Anderson, R. L.; Suarez, G.; Osborne, A. J. G.; Heide, M. K. K.; Merkler, D. J. Characterization and Quantification of the Fatty Acid Amidome. Neuromethods; Springer US, 2020; pp 143–153. doi:10.1007/978-1-0716-0864-7_12
• Ki, D.-W.; El-Desoky, A. H.; Kodama, T.; Wong, C. P.; Ghani, M. A.; El-Beih, A. A.; Mizuguchi, M.; Morita, H. New cytotoxic polyacetylene amides from the Egyptian marine sponge Siphonochalina siphonella. Fitoterapia 2020, 142, 104511. doi:10.1016/j.fitote.2020.104511
• Bode, E.; Heinrich, A. K.; Hirschmann, M.; Abebew, D.; Shi, Y.-N.; Vo, T. D.; Wesche, F.; Shi, Y.-M.; Grün, P.; Simonyi, S.; Keller, N.; Engel, Y.; Wenski, S. L.; Bennet, R.; Beyer, S.; Bischoff, I.; Buaya, A.; Brandt, S. C.; Cakmak, I.; Cimen, H.; Eckstein, S.; Frank, D.; Fürst, R.; Gand, M.; Geisslinger, G.; Hazir, S.; Henke, M.; Heermann, R.; Lecaudey, V.; Schäfer, W.; Schiffmann, S.; Schüffler, A.; Schwenk, R.; Skaljac, M.; Thines, E.; Thines, M.; Ulshöfer, T.; Vilcinskas, A.; Wichelhaus, T. A.; Bode, H. B. Promoter Activation in Δhfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing. Angewandte Chemie (International ed. in English) 2019, 58, 18957–18963. doi:10.1002/anie.201910563
• Bode, E.; Heinrich, A. K.; Hirschmann, M.; Abebew, D.; Shi, Y.; Vo, T. D.; Wesche, F.; Shi, Y.; Grün, P.; Simonyi, S.; Keller, N.; Engel, Y.; Wenski, S.; Bennet, R.; Beyer, S.; Bischoff, I.; Buaya, A.; Brandt, S.; Cakmak, I.; Çimen, H.; Eckstein, S.; Frank, D.; Fürst, R.; Gand, M.; Geisslinger, G.; Hazir, S.; Henke, M.; Heermann, R.; Lecaudey, V.; Schäfer, W.; Schiffmann, S.; Schüffler, A.; Schwenk, R.; Skaljac, M.; Thines, E.; Thines, M.; Ulshöfer, T.; Vilcinskas, A.; Wichelhaus, T. A.; Bode, H. B. Promoter Activation in Δhfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing. Angewandte Chemie 2019, 131, 19133–19139. doi:10.1002/ange.201910563
• Szabó, T.; Dancsó, A.; Ábrányi-Balogh, P.; Volk, B.; Milen, M. First reported propylphosphonic anhydride (T3P®) mediated Robinson–Gabriel cyclization. Synthesis of natural and unnatural 5-(3-indolyl)oxazoles. Tetrahedron Letters 2019, 60, 1353–1356. doi:10.1016/j.tetlet.2019.04.024
• McAlpine, J. B.; Chen, S.-N.; Kutateladze, A. G.; MacMillan, J. B.; Appendino, G.; Barison, A.; Beniddir, M. A.; Biavatti, M. W.; Bluml, S.; Boufridi, A.; Butler, M. S.; Capon, R. J.; Choi, Y. H.; Coppage, D.; Crews, P.; Crimmins, M. T.; Csete, M.; Dewapriya, P.; Egan, J. M.; Garson, M. J.; Genta-Jouve, G.; Gerwick, W. H.; Gross, H.; Harper, M. K.; Hermanto, P.; Hook, J. M.; Hunter, L.; Jeannerat, D.; Ji, N. Y.; Johnson, T. A.; Kingston, D. G. I.; Koshino, H.; Lee, H.-W.; Lewin, G.; Li, J.; Linington, R. G.; Liu, M.; McPhail, K. L.; Molinski, T. F.; Moore, B. S.; Nam, J.-W.; Neupane, R. P.; Niemitz, M.; Nuzillard, J.-M.; Oberlies, N. H.; Ocampos, F. M. M.; Pan, G.; Quinn, R. J.; Reddy, D. S.; Renault, J.-H.; Rivera-Chávez, J.; Robien, W.; Saunders, C. M.; Schmidt, T. J.; Seger, C.; Shen, B.; Steinbeck, C.; Stuppner, H.; Sturm, S.; Taglialatela-Scafati, O.; Tantillo, D. J.; Verpoorte, R.; Wang, B. G.; Williams, C. M.; Williams, P. G.; Wist, J.; Yue, J.-M.; Zhang, C.; Xu, Z.; Simmler, C.; Lankin, D. C.; Bisson, J.; Pauli, G. F. The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research (vol 36, pg 35, 2018). Natural product reports 2018, 36, 35–107. doi:10.1039/c7np00064b
• Anderson, R. L.; Battistini, M. R.; Wallis, D. J.; Shoji, C.; O'Flynn, B. G.; Dillashaw, J. E.; Merkler, D. J. Bm-iAANAT and its potential role in fatty acid amide biosynthesis in Bombyx mori. Prostaglandins, leukotrienes, and essential fatty acids 2018, 135, 10–17. doi:10.1016/j.plefa.2018.06.001
• Reddy, R. J.; Ball-Jones, M. P.; Davies, P. W. Alkynyl Thioethers in Gold-Catalyzed Annulations To Form Oxazoles. Angewandte Chemie (International ed. in English) 2017, 56, 13310–13313. doi:10.1002/anie.201706850
• Reddy, R. J.; Ball‐Jones, M. P.; Davies, P. W. Alkynyl Thioethers in Gold‐Catalyzed Annulations To Form Oxazoles. Angewandte Chemie 2017, 129, 13495–13498. doi:10.1002/ange.201706850
• Broberg, A.; Bjerketorp, J.; Andersson, P. F.; Sahlberg, C.; Levenfors, J. J. Labradorins with Antibacterial Activity Produced by Pseudomonas sp. Molecules (Basel, Switzerland) 2017, 22, 1072. doi:10.3390/molecules22071072

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