Green Simon R, Harrison Justin R, Thompson Stephen, Murugesan Dinakaran, Libardo M Daben J, Engelhart Curtis A, Meshanni Jaclynn, Fletcher Daniel, Scullion Paul, Edwards Darren, Epemolu Ola, Mutter Nicole, Shishikura Yoko, Riley Jennifer, Ioerger Thomas R, Roca Guillén Jose Juan, López Laura Guijarro, Read Kevin D, Barry Clifton E, Schnappinger Dirk, Wyatt Paul G, Boshoff Helena I M, Cleghorn Laura A T
Drug Discovery Unit, Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Tuberculosis Research Section, Laboratory of Clinical Immunology and Microbiology, NIAID, NIH, Rockville Pike, Bethesda, Maryland 9000, United States.
ACS Infect Dis. 2025 Mar 14;11(3):715-726. doi: 10.1021/acsinfecdis.4c00808. Epub 2025 Feb 27.
Although not currently in the infectious disease spotlight, there is still a pressing need for new agents to treat tuberculosis caused by . As there is an ever-increasing amount of clinical resistance to the current drugs, ideally new drugs would be found against novel targets to circumvent pre-existing resistance. A phenotypic growth screen identified a novel singleton, , as an inhibitor of growth. Mechanism-of-action studies determined that targeted Pks13, an essential enzyme in cell wall biosynthesis that, as of yet, has not been targeted by agents in the clinic. The reactive nature of the pentafluorophenyl warhead meant that the molecule was inherently metabolically unstable. A medicinal chemistry optimization program is described that resulted in the identification of a compound that was reactive enough to still inhibit Pks13 and growth while being metabolically stable enough to explore in vivo.
尽管目前结核病并非传染病领域的关注焦点,但对于治疗由……引起的结核病,仍迫切需要新型药物。由于目前临床中对现有药物的耐药性不断增加,理想情况下,应找到针对新靶点的新药以规避已有的耐药性。一项表型生长筛选确定了一种新型单一化合物……作为……生长的抑制剂。作用机制研究表明,……靶向Pks13,这是一种细胞壁生物合成中的关键酶,目前临床药物尚未针对该靶点。五氟苯基弹头的反应活性意味着该分子本质上代谢不稳定。本文描述了一个药物化学优化项目,该项目鉴定出一种化合物,其反应活性足以抑制Pks13和……生长,同时代谢稳定性足以进行体内研究。