Latvian Institute of Organic Synthesis, Riga, Latvia.
Med Res Rev. 2022 Jan;42(1):5-55. doi: 10.1002/med.21803. Epub 2021 Apr 13.
The isolation of the antitumor antibiotic anthramycin in the 1960s prompted extensive research into pyrrolo[1,4]benzodiazepines (PBD) as potential therapeutics for the treatment of cancers. Since then, nearly 60 PBD natural products have been isolated and evaluated with regard to their biological activity. Synthetic studies and total syntheses have enabled access to PBD analogues, culminating in the development of highly potent anticancer agents. This review provides a summary of the occurrence and biological activity of PBD natural products and covers the strategies employed for their total syntheses.
20 世纪 60 年代,抗肿瘤抗生素安曲霉素(anthramycin)的分离促使人们对吡咯并[1,4]苯并二氮杂卓(PBD)进行了广泛的研究,以期将其开发为治疗癌症的潜在疗法。此后,人们已经分离出近 60 种 PBD 天然产物,并对其生物活性进行了评估。合成研究和全合成使人们能够获得 PBD 类似物,最终开发出了高效的抗癌药物。本文综述了 PBD 天然产物的分布和生物活性,并概述了其全合成所采用的策略。