Cui Jerry, Ju Kou-San
Department of Microbiology, The Ohio State University, Columbus, OH 43210, United States.
Department of Microbiology, The Ohio State University, Columbus, OH 43210, United States; Division of Medicinal Chemistry and Pharmacognosy, The Ohio State University, Columbus, OH 43210, United States.
Curr Opin Microbiol. 2025 Jul 11;87:102630. doi: 10.1016/j.mib.2025.102630.
Phosphonate and phosphinate compounds - both natural and synthetic - have given rise to major families of therapeutics and agricultural agents. The antibiotic fosfomycin, the antivirals foscarnet and tenofovir, the bisphosphonates, and the herbicides phosphinothricin and glyphosate all belong to this compound class. The carbon-phosphorus bonds that define these molecules enable chemical mimicry of essential phosphate ester and carboxylate metabolites within metabolism, which is the foundation for their bioactivity. Here, we review examples of C-P compounds in drug discovery. In the first half, we highlight the ongoing development of two phosphonate natural products, both of which were initially discovered as antibiotics: fosmidomycin, which has undergone clinical trials as an antimalarial, and SF-2312, derivatives of which are currently being explored as chemotherapeutics. In the second half, we summarize how the C-P moiety has inspired chemical synthesis of new antimicrobials, immunomodulators, and targeted protein degradation agents.
膦酸酯和次膦酸酯化合物——包括天然的和合成的——催生了主要的治疗药物和农用制剂家族。抗生素磷霉素、抗病毒药物膦甲酸钠和替诺福韦、双膦酸盐以及除草剂草铵膦和草甘膦都属于这一类化合物。定义这些分子的碳-磷键能够在新陈代谢中对必需的磷酸酯和羧酸盐代谢物进行化学模拟,这是它们生物活性的基础。在此,我们回顾药物发现中碳-磷化合物的实例。在前半部分,我们重点介绍两种膦酸酯天然产物的持续研发情况,这两种天然产物最初均作为抗生素被发现:已作为抗疟药物进行临床试验的磷霉素,以及其衍生物目前正在作为化疗药物进行探索的SF-2312。在后半部分,我们总结碳-磷部分如何激发了新型抗菌剂、免疫调节剂和靶向蛋白质降解剂的化学合成。