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四环双哌啶生物碱:结构、仿生合成、合成及生物活性

Tetracyclic Bis-Piperidine Alkaloids: Structures, Bioinspired Synthesis, Synthesis, and Bioactivities.

作者信息

Gómez Stan Iridio, Oceguera Nava Esveidy Isabel, Dadawalla Abbas, Ashong Dennis, Chen Guanglin, Chen Qiao-Hong

机构信息

Department of Chemistry & Biochemistry, California State University, Fresno, CA 93740, USA.

出版信息

Molecules. 2025 Jul 9;30(14):2907. doi: 10.3390/molecules30142907.

Abstract

Tetracyclic bis-piperidine alkaloids (TcBPAs) are structurally complex natural products primarily isolated from marine sponges of the order Haplosclerida. Distinguished by their intricate architecture, TcBPAs feature two central piperidine units linked by dual macrocyclic rings. These unique structural motifs contribute significantly to their biological activities. For example, TcBPAs exhibit antiproliferative activities at low micromolar concentrations across various cancer cell lines, including leukemia, melanoma, breast, colon, fibrosarcoma, and glioblastoma. Despite this promising therapeutic profile, the structural intricacy of TcBPAs has posed considerable challenges to the development of efficient synthetic methodologies, thereby limiting comprehensive exploration and potential clinical advancement. This review highlights recent progress and persisting challenges in the synthesis, structural analysis, and biological evaluation of TcBPAs, underscoring their therapeutic potential in anticancer drug discovery.

摘要

四环双哌啶生物碱(TcBPAs)是结构复杂的天然产物,主要从单轴海绵目(Haplosclerida)的海洋海绵中分离得到。TcBPAs以其复杂的结构而著称,其特征是两个中心哌啶单元通过双大环连接。这些独特的结构基序对它们的生物活性有显著贡献。例如,TcBPAs在低微摩尔浓度下对包括白血病、黑色素瘤、乳腺癌、结肠癌、纤维肉瘤和胶质母细胞瘤在内的各种癌细胞系均表现出抗增殖活性。尽管具有这种有前景的治疗特性,但TcBPAs的结构复杂性给高效合成方法的开发带来了相当大的挑战,从而限制了全面的探索和潜在的临床进展。本综述重点介绍了TcBPAs在合成、结构分析和生物学评价方面的最新进展和持续存在的挑战,强调了它们在抗癌药物发现中的治疗潜力。

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