Mehboob Shahila, Song Jinhua, Hevener Kirk E, Su Pin-Chih, Boci Teuta, Brubaker Libby, Truong Lena, Mistry Tina, Deng Jiangping, Cook James L, Santarsiero Bernard D, Ghosh Arun K, Johnson Michael E
Center for Pharmaceutical Biotechnology, University of Illinois at Chicago, Chicago, IL 60607, United States; Novalex Therapeutics, 2242 W. Harrison, Chicago, IL 60612, United States.
Department of Chemistry, Purdue University, West Lafayette, IN 47907, United States; Department of Medicinal Chemistry, Purdue University, West Lafayette, IN 47907, United States.
Bioorg Med Chem Lett. 2015 Mar 15;25(6):1292-6. doi: 10.1016/j.bmcl.2015.01.048. Epub 2015 Jan 29.
Francisella tularensis, the causative agent of tularemia, presents a significant biological threat and is a Category A priority pathogen due to its potential for weaponization. The bacterial FASII pathway is a viable target for the development of novel antibacterial agents treating Gram-negative infections. Here we report the advancement of a promising series of benzimidazole FabI (enoyl-ACP reductase) inhibitors to a second-generation using a systematic, structure-guided lead optimization strategy, and the determination of several co-crystal structures that confirm the binding mode of designed inhibitors. These compounds display an improved low nanomolar enzymatic activity as well as promising low microgram/mL antibacterial activity against both F. tularensis and Staphylococcus aureus and its methicillin-resistant strain (MRSA). The improvements in activity accompanying structural modifications lead to a better understanding of the relationship between the chemical structure and biological activity that encompasses both enzymatic and whole-cell activity.
土拉弗朗西斯菌是兔热病的病原体,由于其具有被武器化的潜力,构成了重大的生物威胁,是A类优先病原体。细菌的Ⅱ型脂肪酸合成途径是开发治疗革兰氏阴性菌感染的新型抗菌剂的一个可行靶点。在此,我们报告了一系列有前景的苯并咪唑类FabI(烯酰-ACP还原酶)抑制剂通过系统的、结构导向的先导化合物优化策略发展到第二代的过程,以及确定了几个共晶体结构,这些结构证实了设计抑制剂的结合模式。这些化合物显示出改善的低纳摩尔酶活性,以及对土拉弗朗西斯菌和金黄色葡萄球菌及其耐甲氧西林菌株(MRSA)有前景的低微克/毫升抗菌活性。伴随结构修饰的活性改善有助于更好地理解涵盖酶活性和全细胞活性的化学结构与生物活性之间的关系。