Alali F Q, Zhang Y, Rogers L, McLaughlin J L
Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, IN 47907, USA.
Phytochemistry. 1998 Oct;49(3):761-8. doi: 10.1016/s0031-9422(97)00922-9.
Goniotetracin and a mixture of (2,4-cis and trans)-gonioneninone, new, bioactive, mono-tetrahydrofuran (THF) gamma-lactone and ketolactone acetogenins, were isolated from the bark of Goniothalamus giganteus (Annonaceae) by activity-directed fractionation using the brine shrimp lethality test (BST). The structures were elucidated based on spectroscopic and chemical methods. Their absolute stereochemistries were determined by the advanced Mosher ester method. Both showed selective and significant cytotoxicities, comparable to the potency of adriamycin, to the human pancreatic tumour cell line (PACA-2), while goniotetracin and goniothalamicin were comparable to the activity of rotenone against yellow fever mosquito larvae.
通过使用卤虫致死试验(BST)进行活性导向分级分离,从大花哥纳香(番荔枝科)的树皮中分离出了哥纳四环素以及(2,4-顺式和反式)-哥纳烯宁酮的混合物,它们是新型的、具有生物活性的单四氢呋喃(THF)γ-内酯和酮内酯类番荔枝内酯。基于光谱和化学方法阐明了它们的结构。通过先进的莫舍尔酯法确定了它们的绝对立体化学结构。二者对人胰腺肿瘤细胞系(PACA-2)均表现出选择性且显著的细胞毒性,其效力与阿霉素相当,而哥纳四环素和哥纳香霉素对黄热病蚊幼虫的活性与鱼藤酮相当。