Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, P. R. China.
Department of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, Illinois 60612, United States.
Chem Biodivers. 2022 Jun;19(6):e202101004. doi: 10.1002/cbdv.202101004. Epub 2022 May 20.
An undescribed C22-quassinoid named sergeolide A (1) and fifteen known quassinoids (2-16) were obtained from the seeds of Brucea javanica (Simaroubaceae). All chemical structures were established based on spectroscopic data and X-ray diffraction analysis. Sergeolide A (1) is the first example of a naturally occurring C22-quassinoid bearing a butenolide group fused the A ring of the bruceolide skeleton from Brucea genus. And this is the first report of the NMR data for desmethyl-bruceines B (2) and C (3) and the crystal structure for bruceolide (11). In addition, all isolates were evaluated for their anti-pancreatic adenocarcinoma activity by measuring the growth inhibitory of the MIA PaCa-2 cell lines. Consequently, compounds 1, 7-10, and 12-16 exhibited potent anti-pancreatic cancer activity in vitro (IC =0.054∼0.357 μM).
从苦木科鸦胆子属植物鸦胆子(Brucea javanica)的种子中分离得到了 1 个新的 C22 型苦木苦味素类化合物(1)和 15 个已知苦木苦味素类化合物(2-16)。根据波谱数据和 X 射线衍射分析确定了所有化合物的结构。化合物 1 是第一个天然存在的带有丁烯内酯基团的 C22 型苦木苦味素类化合物,其 A 环与鸦胆子属的 bruceolide 骨架相融合。这是首次报道去甲基鸦胆子宁 B(2)和 C(3)的 NMR 数据以及 bruceolide(11)的晶体结构。此外,还通过 MIA PaCa-2 细胞系的生长抑制试验评估了所有分离得到的化合物的抗胰腺癌活性。结果表明,化合物 1、7-10、12-16 具有较强的体外抗胰腺癌活性(IC=0.054∼0.357μM)。