Pedrola Marina, Jorba Marta, Jardas Eda, Jardi Ferran, Ghashghaei Ouldouz, Viñas Miguel, Lavilla Rodolfo
Laboratory of Medicinal Chemistry, Faculty of Pharmacy and Food Sciences and Institute of Biomedicine (IBUB), University of Barcelona, Barcelona, Spain.
Laboratory of Molecular Microbiology & Antimicrobials, Department of Pathology & Experimental Therapeutics, Medical School, Hospitalet de Llobregat, University of Barcelona, Barcelona, Spain.
Front Chem. 2019 Jul 4;7:475. doi: 10.3389/fchem.2019.00475. eCollection 2019.
Novel antibiotic compounds have been prepared through a selective multicomponent reaction upon the known drug Trimethoprim. The Groebke-Blackburn-Bienaymé reaction involving this α-aminoazine, with a range of aldehydes and isocyanides afforded the desired adducts in one-step. The analogs display meaningful structural features of the initial drug together with relevant modifications at several points, keeping antibiotic potency and showing satisfactory antimicrobial profile (good activity levels and reduced growth rates), especially against methicillin-resistant . The new products may open new possibilities to fight bacterial infections.
通过对已知药物甲氧苄啶进行选择性多组分反应制备了新型抗生素化合物。涉及这种α-氨基嗪的格罗布克-布莱克本-比奈梅反应,与一系列醛和异氰化物一步生成了所需的加合物。这些类似物展现出初始药物有意义的结构特征以及在几个位点的相关修饰,保持了抗生素效力并显示出令人满意的抗菌谱(良好的活性水平和降低的生长速率),尤其是对耐甲氧西林菌。这些新产品可能为对抗细菌感染开辟新的途径。