Institute of Traditional Chinese Medicine and Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of Traditional Chinese Medicine and New Drug Research, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Department of Pathogen Biology, Jiangsu Key Laboratory of Pathogen Biology, Helicobacter pylori Research Centre, Nanjing Medical University, Nanjing 211166, China.
Fitoterapia. 2022 Jan;156:105095. doi: 10.1016/j.fitote.2021.105095. Epub 2021 Dec 8.
Marine-derived fungi can usually produce structurally novel and biologically potent metabolites. In this study, a new diketopiperazine alkaloid (1) and two new polyketides (10 and 11), along with 8 known diketopiperazine alkaloids (2-9) were isolated from marine-derived fungus Penicillium sp. TW58-16. Their structures were fully elucidated by analyzing UV, IR, HR-ESI-MS, 1D, and 2D NMR spectroscopic data. The absolute configurations of the new compounds 1, 10 and 11 were ascertained by X-ray diffraction (Cu Kα radiation) and comparing their CD data with those reported. In addition, the antibacterial activities of these compounds against Helicobacter pylori in vitro were assessed. Results showed that compounds 3, 6, 8 and 9 displayed moderate antibacterial activity against standard strains and drug-resistant clinical isolates of H. pylori in vitro. This result demonstrates that diketopiperazine alkaloids could be lead compounds to be explored for the treatment of H. pylori infection.
海洋来源真菌通常可以产生结构新颖和生物活性强的代谢产物。在本研究中,从海洋来源真菌青霉 TW58-16 中分离得到了一个新的二酮哌嗪生物碱(1)和两个新的聚酮(10 和 11),以及 8 个已知的二酮哌嗪生物碱(2-9)。通过分析 UV、IR、HR-ESI-MS、1D 和 2D NMR 波谱数据,充分阐明了它们的结构。通过 X 射线衍射(Cu Kα 辐射)和与文献报道的 CD 数据比较,确定了新化合物 1、10 和 11 的绝对构型。此外,还评估了这些化合物对体外幽门螺杆菌的抗菌活性。结果表明,化合物 3、6、8 和 9 对标准株和体外耐药临床分离株幽门螺杆菌均显示出中等的抗菌活性。这一结果表明,二酮哌嗪生物碱可能是治疗幽门螺杆菌感染的潜在先导化合物。